Medical instrument, ring prosthesis, stent and stented valve

ABSTRACT

A prosthesis includes a tube with a proximal and distal flange around the tube. The distal and proximal flanges have a radial position, projecting radially outward to clamp tissue between the flanges. The flanges include distal flange feet and proximal flange feet. The distal and proximal flange feet bend from the radial position, against a pre-tension of the memory material, to an extended position, in which the distal and proximal flange feet extend in the longitudinal direction of the tube and are fixable there, returning when released to the radial position urged by the pre-tension. The flange feet have on inner sides a filling to increase the clamping force. The flange feet have a concave-curved part extending from the fixed ends of the flange feet. The hollow side of the concave faces the proximal and/or distal flange and the filling is provided in the hollow side of the concave.

The present application relates to inventions in the field of prosthesesand in the field of medical instruments, such as medical instruments forimplanting a prosthesis.

More particularly, this application relates to medical instruments forintervention in, on or near the heart, and/or intervention in or on apassage, such as a blood vessel or hollow organ, through which a bodyfluid, such as blood, flows. The inventions furthermore also relate toprostheses, such as heart valve prostheses, which are understood inevery case to include: so-called ring prostheses, the purpose of whichis to constrict an excessively wide passage near a heart valve, or toconstrict or close a natural or artificially disposed passage in tissue;artificial valve prostheses, which replace a heart valve; mechanicalvalve prostheses, but also biological valve prostheses, includingso-called stented valves and valved stents; and also components of suchprostheses. Furthermore, the inventions also relate to stents andcomponents of the stents. According to the inventions in thisapplication, a prosthesis is also understood to mean a part of aprosthesis.

As far as medical instruments are concerned, the medical instrumentsaccording to the present inventions are in particular also usable as anapplicator for implanting a ‘prosthesis of the type with a tubularelement’ provided with a distal and proximal flange which extend alongthe circumference of the tubular element, the distal flange of which hasflange feet which are bendable from the extended axial position to theradial position. This type of prosthesis will be further referred to inthis application as a ‘prosthesis of the type with a tubular element’for short. In the extended axial position, the distal flange feet extendfrom the tubular element in the distal direction and, in the radialposition, the flange feet extend outwards from the tubular element inthe radial direction. The extended position is a temporary position herewhich normally simplifies the movement to the intended location in thebody. Having arrived at the intended location, the distal flange feetare bent from the extended axial position to the radial position.Attachment to surrounding tissue is effected here in that tissue onwhich the distal flange feet and the proximal flange grip is locatedbetween the distal flange feet in the radial position and the proximalflange. The grip may be a clamping grip, wherein the tissue is clampedlocally between the distal flange feet and proximal flange, or ananchoring grip, wherein the distal flange feet and/or proximal flangeare anchored by means of pins or otherwise to the tissue, or acombination of clamping and anchoring grip. In the case of so-called‘prostheses of the type with a tubular element’, the bending of thedistal flange feet from the extended axial position to the radialposition may be both passive bending and active bending, and also acombined form of passive and active bending. In the case of a‘prosthesis of the type with a tubular element’, the proximal flange mayalso optionally comprise flange feet, referred to as proximal flangefeet, which are to be bent from an extended axial position to a radialposition. This bending of the proximal flange feet can also be bothpassive bending and active bending, and also a combined form of passiveand active bending.

In this application, the term ‘passive bending’ is understood to meanthat a part in a first condition—such as the flange feet in the extendedaxial position—are under a pre-tension which, once released, bends thatpart from the first condition to a second condition—such as the flangefeet from the extended axial position to the radial position. Thebending therefore takes place, as it were, automatically due to thepre-tension. A pre-tension of this type can be implemented in differentways, e.g. by using materials with memory characteristics known to theperson skilled in the art. The necessary metals, metal alloys—such asnitinol—or plastics—such as memory polymers—with memory characteristicsof this type are known to the person skilled in the art. Materials ofthis type can be bent from a specific initial configuration—in this casethe radial position of the flange feet—to a different configuration—inthis case the extended axial position of the flange feet—and can be, asit were, frozen in the different configuration. No mechanical appliancesare then required to maintain the frozen different configuration. The,as it were, ‘frozen’ condition is then releasable, after which thematerial returns to the initial configuration. In many cases, the changefrom the initial configuration to the other configuration is effected ata low temperature, for example by laying the material in ice water, as aresult of which the material becomes “soft” and can be activelydeformed, and the ‘freezing’ is effected by lowering the initialtemperature to below a first threshold value and then to below a secondthreshold value. This is referred to as an S-shaped temperature-force ortemperature-shape curve of the material, wherein the deformation of thematerial under the influence of the temperature change follows anS-shaped line. The undoing of the frozen condition is normally effectedby raising the temperature again to above, in the first instance, thesecond threshold value, and then again to above the first thresholdvalue, wherein the initial configuration is again attained. In medicalapplications, the first threshold value often lies a few degrees belowthe normal body temperature of 37 degrees Celsius, so that the materialin each case has the initial configuration at body temperature. Thefirst and second threshold values may lie close to one another, but inpractice often lie approximately 10 degrees Celsius apart from oneanother. In the case of nitinol, the second threshold value is usuallylower than or around room temperature. In order then to preventpremature release from the ‘frozen condition’ under the influence of theroom temperature or body temperature of the patient, an additionalmechanically removable impediment or a cooling system to maintain alower temperature will often be involved in practice—and also accordingto the invention. Finally, it is noted that, according to the invention,a pre-tension of this type is not only implementable by using materialswith memory characteristics. A pre-tension of this type can also becreated by using a ‘normal’ resilient material which must be held in aresiliently pre-tensioned condition by means of an external mechanical,removable impediment.

In this application, active bending is understood to mean that anexternal force must be exerted to bend a part—in this case normally theflange feet—which is, in a manner of speaking, pushed against the part(the flange feet) or pulled onto the part (the flange feet).

So-called ‘prostheses of the type with a tubular element’, for which themedical instrument according to the invention is usable as anapplicator, are, inter alia, described extensively in earlier PCTapplications of the inventor, i.e. WO 00/24339, WO 00/44311, WO03/003926, WO 03/082121 and WO 2005/092246. These PCT applications areall included by reference in the present application as far as thedetails of the ‘prosthesis of the type with a tubular element’ areconcerned.

First Aspect

According to a first aspect, this application relates to a medicalinstrument. According to the invention, the medical instrument,according to the first aspect, comprises:

-   -   a first rod;    -   a second rod which extends along and parallel to the first rod;    -   a longitudinal centre line defined by the direction in which the        first rod and the second rod extend; and    -   a manipulator.

The manipulator in the case of the instrument according to the firstaspect is usable for manipulating a prosthesis, such as for implanting aprosthesis and/or for creating a passage through tissue and/or fortreating a passage intended for through-flow with blood. If themanipulator of the medical instrument according to the first aspect isintended in particular for the implanting of a prosthesis, the medicalinstrument according to the first aspect is in fact referred to as anapplicator. An applicator of this type is known from WO 03/003926 of theinventor.

In the case of the applicator known from WO 03/003926, a release deviceis involved, comprising a release ring (7) provided on the distal end ofthe applicator. An overlapping position is involved, in which the distalflange feet of the prosthesis to be implanted project into the releasering in order to be held and/or protected by the release ring in theaxial extended position. This release ring can be shifted from theoverlapping position in the distal direction by a release rod (6)distally in relation to another rod, referred to as the carriage tube(4), and can thus be moved away from the distal flange feet, after whichthe distal flange feet lie free and move to the radial position. In WO03/003926, the manipulator is formed by the aforementioned release ring.

Although in WO 03/003926 the release ring has a diameter which is lessthan the internal diameter of the prosthesis to be implanted, so thatthe release ring lying distally from the prosthesis, followingimplantation of the prosthesis, can be retracted in the proximaldirection through the prosthesis, this release ring is relatively largeand, when the instrument is retracted following implantation of theprosthesis, can easily remain caught up somewhere. Furthermore, in thecase of this release ring, the flange feet pointing radially outwards inthe fixed condition must be bent beyond the purely axial position sothat they point slightly radially inwards. The reason for this is thatthe release ring cannot otherwise have a diameter less than the diameterof the passage through the prosthesis. Furthermore, the manipulator fromWO 03/03926, i.e. the release ring from WO 03/003926, is passive in thesense that it can only release extended flange feet, but otherwise ishardly or not deployable or usable for other purposes.

According to the first aspect, the object of the present application is,inter alia, to provide an improved medical instrument, comprising: afirst rod, a second rod which extends along and parallel to the firstrod; a longitudinal centre line defined by the direction in which thefirst rod and the second rod extend; and a manipulator device.

This object is achieved according to the first aspect by providing amedical instrument, comprising:

-   -   a first rod;    -   a second rod which extends along and parallel to the first rod;    -   a longitudinal centre line defined by the direction in which the        first rod and the second rod extend; and        a manipulator;        wherein the manipulator according to the invention comprises at        least a plurality of fingers, each with a first finger end and a        second finger end; wherein the second finger ends are free ends;        wherein the first finger ends of these aforementioned plurality        of fingers are supported on the second rod in such a way that        the fingers of the aforementioned plurality of fingers, by        moving the second rod in relation to the first rod, can be        operated in order to be displaced from a first position to a        second position; and wherein the distance from the free ends of        the fingers to the longitudinal centre line in the first        position is different compared with the second position.

Two options are available here according to the first aspect: thedistance from the free ends of the fingers can be greater in the firstposition than in the second position or, conversely, the distance fromthe free ends of the fingers can be greater in the second position thanin the first. It is furthermore noted in a general sense in relation tothis application that, viewed from an initial condition in which thedistance from the free ends of the fingers to the longitudinal centreline is relatively great, changing to a different condition in whichthis distance is relatively—in relation to the initialcondition—smaller, the change in distance can be referred to by theterms ‘reduction in the span of the fingers’ or ‘span reduction’ used inthis application.

By designing the manipulator as a plurality of fingers with free ends,from which the distance to the longitudinal centre line is variable, itis possible to move the fingers from a first position with, in thisexample, a great distance to the longitudinal centre line to a secondposition with, in this example, a small distance to the longitudinalcentre line (great distance and small distance are meant here asrelative in relation to one another and do not indicate the magnitude ofthese distances). It is therefore possible, if this medical instrumentis used as an applicator, to reduce the manipulator in size afterdelivering/implanting the prosthesis, thereby making it easier toretract, possibly through the implanted/delivered prosthesis 1. However,it is also possible, in the case of the medical instrument according tothe first aspect, to use the manipulator as an attribute for performingan intervention. For example, one or more appliances for anintervention, such as scalpels and/or a punch unit, can be provided onthe free finger ends. It is then, for example, possible to move themanipulator, in a reduced-size condition, to the intervention locationand there to increase the circumference—or the span—of the manipulator.Scalpels or a punch unit can therefore be moved, while avoiding contactwith surrounding tissue, to the intervention location, where they can beincreased to the required size in order to be able to treat surroundingtissue. However, the free finger ends may also comprise other appliancesfor an intervention. The free finger ends can also be simply usedwithout scalpels as pressure units in order, for example, to cause theexpansion of a stent or other prosthesis or an original valve, if this,for example, is diseased or constricted. According to the prior art, aballoon is normally used for an expansion of this type. The plurality offingers according to the first aspect therefore provides an alternativeto this.

According to one embodiment of the first aspect, the first rod and thesecond rod are shiftable in relation to one another in the longitudinaldirection of the longitudinal centre line for the aforementionedoperation of the fingers. It is therefore possible, by shifting thefirst rod and the second rod in relation to one another, to subject thefingers to a longitudinal displacement in the direction of thelongitudinal centre line of the instrument and/or to a transversedisplacement in a direction across the longitudinal centre line of theinstrument and/or to a rotation around the longitudinal centre line ofthe instrument. This may involve:

-   -   only a longitudinal displacement; or    -   only a transverse displacement; or    -   only a rotation; or    -   a combination of longitudinal displacement and/or transverse        displacement and/or rotation.        A combination of this type may involve a combined displacement,        i.e. two or three of the aforementioned types of displacement        take place simultaneously, and also a sequential displacement,        wherein two or three of the aforementioned types of displacement        can take place successively in any required sequence.

According to another further embodiment of the first aspect, the firstrod and the second rod are rotatable in relation to one another aroundthe longitudinal centre line for the aforementioned operation of thefingers. The first rod and second rod may be interconnected hereaccording to a further embodiment by means of a screw thread. Rotationof the one rod in relation to the other rod then results in atranslation of the one rod in relation to the other rod along the centreline. This translation can then in turn be used to displace the fingersalong the longitudinal centre line. Whether or not in combination with ascrew thread connection between the first and the second rod, it is alsopossible, in the case of rotation of the first rod and the second rod inrelation to one another around the longitudinal centre line, to displacethe fingers along an arc.

According to a further embodiment of the first aspect, in the secondposition or the first position, the distance from the free ends of thefingers to the second rod is at most 90%, in particular at most 80%,such as at most 75% or at most 70%, of the distance from the free endsof the fingers to the second rod in the other of these two positions. Inother words, a span reduction is involved in changing from a greatdistance to smaller distance. In parallel with the above, this spanreduction of the free ends of the fingers, changing from the firstposition to the second position (or conversely changing from the secondposition to the first position), is respectively at least 10%, inparticular at least 20%, such as at least 25% or at least 30%. In thecase of an expandable prosthesis, a span reduction of up to 90% orpossibly 80% will normally be sufficient since the expansion of theprosthesis following delivery thereof already provides the requiredadditional space for the retraction of the manipulator. In situations inwhich the manipulator is used to expand or support a prosthesis, it isnormally useful if the size of this manipulator can increasesubstantially or even very substantially (speaking in the terminology ofspan reduction, this is then to be regarded as returning from thewidened condition to the original—or even narrower—condition). The sameapplies even if the manipulator is used as an attribute for performingthe intervention.

According to a further embodiment of the first aspect, the plurality offingers is disposed in a distributed manner over the circumferencearound the longitudinal centre line.

According to a further embodiment of the first aspect, the free, secondfinger ends can be provided with a hook with a hook opening which opensin the direction of the first finger ends. The fingers can therefore,for example, project from the proximal side of a prosthesis along theinside of the prosthesis to the distal side of the prosthesis in orderto grip from the inside on pins or flange feet of the prosthesispointing in the distal direction.

According to a further embodiment of the first aspect, the medicalinstrument comprises a tensioning system which acts on the fingers topre-tension them for displacement from the first position to the secondposition. If the fingers are in the first position, the tensioningsystem under pre-tension then acts on the fingers in one direction—thedirection of the pre-tension—in such a way that the tensioning systemdrives or at least is inclined to drive the fingers from the firstposition to the second position. The fingers can also be temporarilyprevented from moving from the first to the second position, for exampleif they are first restrained by a physical obstacle (restrainingelement) which is to be removed. An obstacle of this type could, forexample, be a prosthesis or a part of a prosthesis, but may also formpart of that part of the medical instrument which is removed once morefrom (the organ or the body of) the patient following the intervention.

According to a further embodiment of the first aspect, the tensioningsystem comprises a resilient element provided in the circumferentialdirection of the instrument along the fingers. A resilient element ofthis type, such as an elastic resilient element, may, for example, beformed by a ring of an elastic material, such as an elastic plastic. Aresilient element may also be designed in other ways. A resilientelement may, for example, also have the configuration of an annularspiral spring. A resilient element of this type may be provided on theoutside of the fingers, but may also pass through the fingers or beprovided on the inside of the fingers.

According to a further embodiment of the first aspect, the distance fromthe free ends of the fingers to the longitudinal centre line is greaterin the first position than in the second position.

According to a further embodiment of the first aspect, the fingers aremovable from the first position to the second position and from thesecond position to a third position, wherein the distance from the freeends of the fingers to the longitudinal centre line in the firstposition is less than in the second position, and wherein the distancefrom the free ends of the fingers to the longitudinal centre line in thethird position is less than in the second position. It is thereforepossible for the fingers to be in an initial position, the firstposition, when the instrument is brought to the target location in thebody of the patient—referred to as the intervention location forshort—and, at the ‘intervention location’, to change from the initialposition, i.e. the first position, first to a wider position, i.e. thesecond position, then to return from the wider position, i.e. the secondposition, to a narrower position, i.e. the third position, in which thespan determined by the fingers is again smaller. The span may possiblybe slightly greater in the third position than in the first position.However, this span in the third position will, in particular, be equalto or even less than the span in the initial position, i.e. the firstposition. This is useful, for example, if the medical instrument is usedas an applicator for an expandable prosthesis. In this case, theprosthesis is then brought to the intended location with the fingers inthe first position, the prosthesis can then be allowed to expand in acontrolled manner at the intended location, i.e. by increasing the spanof the fingers in a controlled manner, in order then to return thefingers, after the prosthesis has been detached from the fingers, to aposition with a smaller span, the third position. The instrument, inparticular the manipulator thereof, can then be easily removed from thepatient, possibly even through the expanded prosthesis.

In a further embodiment of the first aspect, the fingers are attached atthe first finger ends in a pivotable manner, such as in a hinged manner,via a pivot attachment to the second rod. The free finger ends cantherefore pivot around the pivot attachment in order to change thedistance from the respective free finger ends to the longitudinal centreline. The transverse dimensions of the manipulator, i.e. the dimensionsviewed across the longitudinal centre line of the medical instrument,are largely determined in the part of the medical instrument in thevicinity of the manipulator by precisely this manipulator, and indeedalso the (span of the) fingers thereof. By attaching the first fingerends pivotably by means of a pivot attachment to the second rod, it ispossible to manipulate the distance from the second finger ends, i.e.the free ends of the fingers, in relation to the longitudinal centreline of the medical instrument over a great distance, i.e., viewedacross the longitudinal centre line of the medical instrument, thedifference in the distance from the second finger ends to thelongitudinal centre line in the second position may be significantly toeven substantially greater than in the first position (or, conversely,significantly or even substantially greater in the first position thanin the second position). By moving the second rod in relation to thefirst rod, which may involve rotation and/or translation, the secondfinger ends, i.e. the free ends of the fingers, can be moved from afirst position to the second position. In the case of a so-called‘prosthesis of the type with a tubular element’, the first position may,for example, be a position in which the free finger ends, viewed in aradial direction, overlap the distal flange feet from the distal side,and the second position will then be a release position, in which thisoverlap has been undone. If the medical instrument is then operated fromthe proximal side by an operator, such as a doctor, and protrudes on thedistal side through a prosthesis to be implanted, so that themanipulator lies on the distal side of the prosthesis, it is now verysimple to retract the medical instrument in the proximal direction oncethe prosthesis has been detached. The part of the medical instrument, inparticular the manipulator, which, prior to the detachment, liesdistally from the prosthesis, can in fact be substantially reduced insize, viewed in the radial direction, and can therefore easily beretracted through the prosthesis. This is also already possible in WO03/003926, but this is achieved here by means of a release ring, thediameter of which is less than the diameter of the prosthesis, but thediameter of which is furthermore not variable. Consequently, the distalflange feet must bend over a relatively great angular distance, to suchan extent that they converge in the distal direction. At any rate, therelease ring, having been bent away from the overlapping position,cannot otherwise be retracted through the prosthesis. Due to the factthat, in WO 03/003926, the distal flange feet must therefore bend over arelatively great angular distance in order to return to the radialposition, it is not possible to work here with distal flange feet which,prior to implantation/detachment, run purely axially in the overlappingposition or are even designed to be conically widening in the radialdirection. Furthermore, it is not always possible to bend the distalflange feet so that they converge inwards beyond the axial direction. Aprosthesis, particularly a valve prosthesis, may therefore even preventthis or make it impossible. For example, the struts of a stentedbiological mitral heart valve prosthesis located in a prosthesis of thetype with a tubular element will be able to project on the distal sideof this tubular element, where they can prevent the bending of thedistal flange feet beyond the axial direction. Furthermore, the furtherthe distal flange feet are bent from the radial initial position, theless close they will be able to return in this radial initial positionunder the influence of the spring action. By then, according to thefirst aspect, designing the free, second finger ends as pivotable inrelation to the first finger ends and by taking the distance of thesecond, free finger ends on the longitudinal centre line of the medicalinstrument in the second position as smaller than in the first position,i.e. span reduction, a design is obtained in a simple manner wherein themanipulator, reduced in span, can be retracted from (an organ orotherwise from the body of) the patient through the prosthesis. The termpivotable is understood here according to the first aspect to mean therelative movement of the free second finger ends in relation to thefirst finger ends. According to the first aspect, the ‘pivot movement’may be a pure rotation movement with the first finger ends as the pointof rotation, for example if the fingers in the case of the first fingerends are designed as hinged, but, according to the first aspect, thismay equally involve a translation movement, a combined rotation andtranslation movement or otherwise.

According to a further embodiment of the first aspect, the distance fromthe pivot attachment of the first finger ends to the longitudinal centreline is unchanging.

According to another further embodiment of the first aspect, the pivotattachment comprises a hinge. According to a further embodiment, thehinge may comprise a convex part and a corresponding concave receptaclefor the convex part. According to another further embodiment, thefingers may be provided here in each case with the aforementionedconcave receptacle. According to the first aspect, a hinge may also beimplemented in a different manner. Thus, the fingers in the case of thefirst finger ends may be provided with a bore through which a ringpasses. The fingers are then all attached in a hinged manner to thering. This ring then extends here around the longitudinal centre lineand is then carried by the first rod.

According to a further embodiment of the first aspect, each fingerfurther comprises an inner longitudinal side facing the longitudinalcentre line, and an outer longitudinal side facing away from thelongitudinal centre line: and the medical instrument further comprises:

-   -   an inner guide provided between the longitudinal centre line and        the inner longitudinal side of the fingers; and    -   an outer guide, wherein the fingers are provided between the        outer guide and the longitudinal centre line;        wherein the first rod carries the inner guide and the outer        guide; wherein each finger has a first curved zone which        determines a first finger part which extends from the first        finger end to the first curved zone, and a second finger part        which extends from the first curved zone to the free end of the        finger; wherein, viewed from the first finger ends to the second        finger ends, the fingers in the first curved zone bend away from        the longitudinal centre line; and wherein, in the second        position, the outer guide grips on the outer longitudinal side        of the second part of the fingers in order to hold together the        fingers in the second position. Due to the fact that the fingers        in the case of the first curved zone stand further radially        outwards, it becomes possible to implement a relatively large        radial span with the fingers without the radial size of the        remainder of the medical instrument having to be large. The        medical instrument can thus be kept relatively slim, while only        the fingers, as a result of the first curved zone, enable a        relatively large radial span. The first curved zone, interacting        with the inner guide and the outer guide, furthermore readily        enables the fingers to be reliably controlled in their position        by means of the inner and the outer guide. In the second        position, the outer guide ensures that the fingers are reliably        held together in a position with a small span.

According to a further embodiment of the first aspect, the inner guidegrips here, in the first position, on the inner longitudinal side of thefirst finger part of the fingers. It is thus ensured that, in the firstposition, the fingers are held outwards, i.e. are held with a greaterspan. The fingers, or at least the free ends thereof, are, as it were,pushed away from the longitudinal centre line.

According to another further embodiment of the first aspect, the innerlongitudinal side of the first and/or second finger part of the fingerslies here, in the second position, free from the inner guide.

According to another further embodiment of the first aspect, the outerlongitudinal side of the first finger part of the fingers lies here, inthe first position, free from the outer guide.

According to another further embodiment of the first aspect, the outerguide grips here, in the first position, on the outer longitudinal sideof the first finger part of the fingers. Here, in the first position,the outer longitudinal side of the second finger part of the fingers mayoptionally lie free from the outer guide.

According to a further embodiment of the first aspect, the inner guidegrips here, in the second position, on the inner longitudinal side ofthe first and/or second finger part of the fingers. Thus, in the secondposition, a confinement of the fingers between the inner guide and theouter guide can be implemented, as a result of which the fingers areheld immovably. Here, in the second position, the inner longitudinalside of the first finger part of the fingers may optionally lie freefrom the inner guide.

According to a further embodiment of the first aspect, the fingers inthe aforementioned first curved zone show a curve of at least 30°, inparticular a curve of at least 45°, such as a curve of 50° or more. Alarge span can thus be implemented for the fingers in the wide positioncompared with a substantially reduced span in the narrow position.

According to a further embodiment of the first aspect, the fingers mayshow a kinked shape in the first curved zone, at least on the innerlongitudinal side of the fingers. A kinked shape creates the possibilityfor the fingers, in the case of a relatively small displacement alongthe longitudinal centre line of the instrument, to make a relativelylarge pivot swing.

According to a further embodiment of the first aspect, the first guideand the outer guide may be immovable in relation to one another. Thefirst guide and outer guide can therefore both be immovably attached tothe first rod.

According to a further embodiment of the first aspect, the inner guideis designed, with the aforementioned movement of the first rod inrelation to the second rod, in such a way that the fingers move to thefirst position in order to guide the free ends of the fingers in aradially outward direction in relation to the longitudinal centre line.It is thus possible, with the aid of fingers, to exert a radiallyoutwardly directed compressive force on an object. It is thus possible,for example, in the case of a so-called ‘prosthesis of the type with atubular element’, to draw the fingers, from the position in which theyoverlap the flange feet from the outside, viewed in the radialdirection, firstly, in the longitudinal direction of the instrument,away from the flange feet, and therefore to undo the overlappingcondition, and then to push these flange feet from the inside with theaid of the fingers from an extended position to the radial position, orat least to support the movement from an extended position to the radialposition.

According to a further embodiment of the first aspect, the outer guideis formed by a side of an annular edge provided on the first rod andfacing towards the free ends of the fingers, for example formed by aring or sleeve. It is thus possible to hold the fingers reliablyconstrained in the second position, at any rate perhaps with an annularelement around them. A sleeve offers the additional advantage that itcan entirely or partially protect the fingers.

According to a further embodiment of the first aspect, a slit is locatedin the first position between the fingers and the inner guide, with aradial size such that, with the aforementioned movement of the first rodin relation to the second rod in such a way that the fingers move in thedirection of the first position, the free ends of the fingers approachthe prosthesis from the inside thereof. It is thus possible, followingthe release of the flange feet, to support the flange feet during themovement from the extended position to the radial position. After thefingers, moving from the first position to the second position, havebeen pushed away from the flange feet, they will come to lie closer tothe longitudinal centre lines of the instrument as a result of the slitand, on returning in the direction of the first position, will approachthe flange feet from the inside.

According to a further embodiment of the first aspect, the outer guideextends around the longitudinal centre line and preferably has adiameter which is smaller than the internal diameter of the prosthesis.It is thus possible, even in the case of a non-expanding prosthesis, tomove the part of the medical instrument where the fingers are locatedthrough the prosthesis.

It is noted that, according to the first aspect, the fingers can also bedesigned to be displaceable in a manner which differs from the pivotablemanner described above. The pivotable manner described above maypossibly be used in combination with such a different manner ofdisplaceability. Examples of a different manner of displaceability ofthis type are discussed below.

According to a further embodiment of the first aspect, the second rodhas a first conical guide surface; and the fingers of the aforementionedplurality of fingers have a guide part at the first finger ends which,through operation of the first rod in relation to the second rod, isshiftable along and in contact with the first conical guide surface todisplace the fingers from the aforementioned first position to theaforementioned second position, wherein the distance from the guideparts to the longitudinal centre line in the first position is differentcompared with the second position. The first conical guide surface andthe fingers shiftable along it can be jointly referred to as a head. Inthis embodiment, it is noted that it is also possible according to thefirst aspect to provide the medical instrument according to the firstaspect with two of these heads. These can then be provided in line withone another, with an interval after one another along the longitudinalcentre line of the medical instrument, and the conical guide surfacescan be pointed here in the same direction.

The span of the fingers can therefore be adjusted by supporting thefingers on an oblique guide surface and by displacing them along thatoblique guide surface. In the event of upward sliding along the conicalguide surface, the span of the fingers increases. In the event ofdownward sliding along the conical guide surface, the span of thefingers decreases. If required, the fingers can additionally bepivotable, wherein they will be pivotable in particular in relation tothe guide part.

According to a further embodiment of the first aspect, the guide part ofan aforementioned finger and the remainder of an aforementioned fingerare rigid in relation to one another. This is understood to mean thatthe guide part and the remainder of the finger are immovable in relationto one another. The remainder of the aforementioned finger willtherefore not then be pivotable in relation to the guide part. Theincrease or decrease in the span of the fingers will then take place bymeans of a pure translation movement of the fingers, said translationmovement being oblique in relation to the longitudinal centre line ofthe medical instrument according to the conicity of the guide surface.

According to a further embodiment of the first aspect with a firstconical guide area, the distance from the fingers to the longitudinalcentre line in the second position may be greater than in the firstposition. This means that an increase in the span of the fingers takesplace if the fingers move from the first position to the secondposition. The fingers can therefore accompany the expansion of aprosthesis without the fingers first having to have released theprosthesis. However, this embodiment is also very readily applicable ifthe medical instrument is required to exert a radial expansion force onan object, such as a prosthesis, or if the medical instrument isrequired to create or widen a passage. In this latter case, the fingers,in particular on the free ends, will be able to be provided with one ormore cutting elements.

According to another further embodiment of the first aspect with a firstconical guide surface, the fingers can be slideable from the secondposition, along and in contact with the guide surface, back in thedirection of the first position. The sliding back in the direction ofthe first position can possibly even take place beyond the firstposition. If the span of the fingers in the second position is greaterthan in the first position, the fingers can therefore end in a thirdposition, in which the span of the fingers is smaller than in the firstposition. If required, the opposite is also possible, i.e. the fingerscan be reduced in span from the first position to a second position inorder then to be increased in span once more from the second position inthe direction of the first position or even beyond the first position.The situation wherein the span of the fingers in the first position issmaller than in the second position and sliding back then takes placefrom the second position in the direction of the first position willoccur in particular if the medical instrument is used as an applicatorfor expandable prostheses. Fingers can then first expand with theprosthesis to allow the expansion to take place in a controlled mannerin order then, once the prosthesis has been released, to return to aposition with a span smaller than in the second position, in particularto return to a position with a span even smaller than in the firstposition. It is thus simple, once the prosthesis has been implanted, toretract the medical instrument once more from the patient. However, thisembodiment will also be very suitable if the medical instrument is usedas an instrument to create or widen a passage.

According to a further embodiment of the first aspect with a firstconical guide surface, the fingers extend parallel to the longitudinalcentre line. If the fingers, with at least a part which is adjacent tothe free end of the fingers, extend parallel to the longitudinal centreline, they will be able to grip the object, such as a prosthesis, firmlyfrom the outside, taking up relatively little or minimal space.

According to a further embodiment of the first aspect, with a firstconical guide surface, the medical instrument further comprises a secondconical guide surface (which may be provided on a third rod) and asecond plurality of fingers, each with a first finger end and a secondfinger end, wherein the second finger ends of the second plurality offingers are free ends; wherein the fingers of the second plurality offingers have a guide part at the first finger ends which is shiftablealong and in contact with the second conical guide surface from a firstposition to a second position, in which the distance from the guideparts of the second plurality of fingers to the longitudinal centre lineis different compared with the first position; wherein the first andsecond conical guide surfaces are disposed as mirrored in relation toone another, such as facing towards one another; and wherein the freeends of the first plurality of fingers are pointed towards the free endsof the second plurality of fingers, and the free ends of the secondplurality of fingers are pointed towards the free ends of the firstplurality of fingers. If the first plurality of fingers and theassociated first conical guide surface are referred to as a first headand the second plurality of fingers and the associated second conicalguide surface are referred to as a second head, this embodiment can bereferred to as a design with a mirrored double head. This embodimentwith a mirrored double head makes it possible to grip, in particular togrip around, an object, such as a prosthesis, from two opposite sides,by means of the first and second plurality of fingers pointed towardsone another. The conical guide surfaces which are similarly pointedtowards one another make it possible here to cause the fingers to varyin span simultaneously in the same direction. Depending on the conicityof the first and second guide surfaces, the fingers will then even beable to move to the same extent. It is noted that it is also possible,according to the first aspect, to provide the medical instrumentaccording to the first aspect with two mirrored double heads. These maythen be provided in line with one another, with an interval behind oneanother along the longitudinal centre line of the medical instrument.

In the embodiment of the first aspect with a first and second conicalguide surface, the first rod can be connected to the first and/or secondplurality of fingers for the operation thereof. Simultaneous operationof the first and the second plurality of fingers is thus possible bymoving the first rod in relation to the second rod.

According to a further embodiment of the first aspect, with a first andsecond conical guide surface, the medical instrument further comprises athird rod which extends along the second rod and is connected to thesecond plurality of fingers for the operation thereof. It is thus madepossible for the second plurality of fingers to be operatedindependently from the first plurality of fingers by means of the thirdrod. This furthermore does not prevent the second plurality of fingersfrom also being connected to the first rod for the operation thereof. Itis therefore then possible for the second plurality of fingers to bemovable by the first rod and/or by the second rod.

According to a further embodiment of the first aspect, the first rod isprovided with a slotted element with slots which extend in thelongitudinal direction of the first rod; the fingers of anaforementioned plurality of fingers extend in each case through anaforementioned slot; in the one of the aforementioned first and secondpositions, the free ends of the fingers of this plurality of fingersproject outwards from the slots; and, in the other of the aforementionedfirst and second positions, the free ends of these fingers are entirelysunk into the slots. In the event that more of a plurality of fingers isprovided, the further plurality or the remaining pluralities of fingersmay also have an associated slotted element. This may possibly be thesame slotted element or a different slotted element. In the case ofseveral pluralities of fingers, it is furthermore also conceivable thatonly the first plurality of fingers or the second plurality of fingershas an associated slotted element. The slotted element creates thepossibility that the fingers, once they have performed their task, suchas the holding of a prosthesis or the creation or widening of a passage,are retracted entirely into the closed element, thereby also preventingthese fingers, when the medical instrument is retracted, for examplefollowing the intervention, from being able to damage surroundingtissue. Damage may easily occur if the free finger ends are providedwith cutting elements, but, even if they carry no cutting elements,damage may easily occur merely through contact of the free finger endswith surrounding tissue. Retraction of the medical instrument is thusconsiderably simplified.

According to a further embodiment of the first aspect with a slottedelement, the slots have slot bases which are designed as guide surfacesto guide the free finger ends in a radial direction in the event ofdisplacement of the second rod in relation to the first rod. The slotbases may be conical or tapered, but may also run along a curved and/orstaggered line. By designing the slot bases as guide surfaces for thefree ends of the fingers, a guiding of the fingers, controlled in aradial direction, is possible in the event of increasing or decreasingof the span thereof.

According to a further embodiment of the first aspect with a slottedelement, in the one of the aforementioned first and second positions, inwhich the free finger ends contact the outside of a hollow prosthesisprovided on the instrument, between the fingers and the slot bases, aslit is provided with a radial size such that, in the event of movementof the fingers from the other of the aforementioned first or secondpositions in the direction of the one of the aforementioned first orsecond positions, the free finger ends approach the hollow prosthesisprovided on the instrument from the inside. It is thus possible, afterthe prosthesis has first been released by the fingers, to then use thefingers to push from the radial inside against the prosthesis or a partthereof, for example in order to cause the prosthesis to expand or topress on the flange feet thereof or to push them to a radial position.The slit ensures here that the fingers, which, viewed in a radialdirection, first overlap the prosthesis from the outside, once thisoverlapping condition has been undone, can approach the prosthesis orcomponents thereof from the inside.

According to a further embodiment of the first aspect, the medicalinstrument according to the first aspect further comprises a stop, suchas a support ring, which, in the case of a prosthesis provided on theinstrument, is located proximally from the prosthesis, and is designedto prevent shifting of the prosthesis in a proximal direction along theinstrument. In a corresponding manner, it is also possible for theinstrument, in addition to the aforementioned stop or separately fromthe aforementioned stop, to comprise a further stop, such as a supportring which, in the case of a prosthesis provided on the instrument, islocated distally from the prosthesis, and is designed to preventshifting of the prosthesis in a distal direction along the instrument.If a part of the medical instrument is displaced through the prosthesis,a stop of this type can prevent the prosthesis from also being carriedalong by the part moving through the prosthesis and also from beingdisplaced in an unwanted manner.

In the embodiment of the first aspect with a stop, the stop may be asupport ring which is attached to the first rod by means of a number,such as 2 or 3, of support arms disposed in a distributed manner overthe circumference of the first rod. The stop can thus be prevented fromobstructing the operator's view of the prosthesis. Separately therefrom,these support arms create space to accommodate a part of the prosthesiswhen the latter is loaded onto the applicator. This is important, forexample, in the case of what is referred to by the person skilled in theart as a ‘stented valve’. The stented valve is normally made frombiological tissue, such as bovine of porcine tissue, wherein the valveis held ‘upright’ by means of a set of struts. The set of strutsnormally consists of a frame of metal or plastic, wherein the locationswhere the valve flaps coincide (referred to as ‘commissures’) are heldupright in order to prevent the valve from collapsing. Particularly ifthe struts of a stented valve of this type point in the proximaldirection, as may be the case, for example, with a stented aortic valve,it is expedient to extend the width and length of the support arms insuch a way that no direct contact occurs between the medical instrumentand a valve of this type.

As well as the ‘stented valve’ described above, a stent also existswhich is referred to by the person skilled in the art as a ‘valvedstent’. A valved stent is primarily a stent in the sense of anexpandable and or compressible, normally tubular, element, usually inthe form of a meshed structure, in which valve tissue is attached, inmost cases by means of adhesions. The stent then automatically holds thecommissures extended or upright.

According to a further embodiment of the first aspect, the instrumentcomprises, in use, a proximal end pointed away from the patient and, inuse, a distal end pointed towards the patient, and the plurality offingers is provided at the distal end. The terms distal and proximal aretherefore defined here from the perspective of the operator. Close tothe operator is proximal, and far away from the operator is distal. Inrelation to the patient, this is then precisely the opposite, i.e.distal is directed towards the patient, and proximal is directed awayfrom the patient.

According to a further embodiment of the first aspect, the plurality offingers here comprises a first plurality of fingers, also referred to asthe distal plurality of fingers, of which the first finger ends facetowards the distal end of the instrument, and the second finger endsface towards the proximal end of the instrument, and the distance fromthe free ends of the fingers of the first plurality of fingers to thesecond rod in the first position is greater than in the second position.In the case of use with a prosthesis, the medical instrument, from theperspective of the operator, will generally project here through theprosthesis, and the fingers, from their non-free end which is supportedon the first rod, will point towards the operator with their free endsin order to be able to grip the prosthesis from the distal side thereoffacing away from the operator. Following detachment of the prosthesis,it will be then be possible to return the fingers from a large span toa—relatively in relation to the aforementioned large span—small(er) spanin order to be retracted through the prosthesis in the proximaldirection. In the case of use as an instrument, for example to widen apassage, it is therefore possible to work on the passage from the distalside facing away from the operator and, on completion of said work, toreturn the fingers to a smaller span in order to be able to retract themsimply through the passage.

According to a further embodiment of the first aspect, wherein themedical instrument is used in particular for implanting a prosthesis, inthe second position, the largest diameter defined by the first pluralityof fingers is smaller than the internal diameter of the prosthesis, inparticular smaller than the internal diameter which the prosthesis hasafter it has been detached from the instrument. Retraction of the firstplurality of fingers from the distal side of the prosthesis through theprosthesis to the proximal side can therefore be carried out simply andwithout damaging the prosthesis.

According to a further embodiment of the first aspect, the second rod isdisplaceable in the distal direction in relation to the first rod forthe purpose of operating the fingers of the first plurality of fingers.

According to a further embodiment of the first aspect, the fingers ofthe first plurality of fingers, viewed from the distal end to theproximal end, are kinked in a second curved zone in a radially inwarddirection, wherein this second curved zone is, in particular, such thatthe part of the fingers of the first plurality of fingers which islocated on the proximal side of the second curved zone can extendparallel to the longitudinal direction of the instrument, whereas,viewed from the first finger ends of the first plurality of fingers inthe direction of the second curved zone, the part of the fingers of thefirst plurality of fingers which is located on the distal side of thesecond curved zone protrudes in a radially outward direction. The partof the fingers protruding in a radially outward direction ensures alarge span here, whereas the part extending, in particular, parallel tothe longitudinal direction of the instrument enables a reliable grip ona prosthesis carried by the instrument or, in the case of other use, forexample, readily enables the performance of work on the inner wall of apassage. Due to the part extending parallel to the longitudinaldirection of the instrument which is formed by the part from the secondcurved zone to the second finger end, this embodiment is very suitable,in particular, for implanting a stent. According to the prior art, it iscustomary for stents to be delivered in a sleeve to the interventionlocation. The sleeve is then retracted in situ and the stent expands. Ifthe stent is not positioned at precisely the correct location and thesleeve has already been retracted (too far), the stent can then nolonger be repositioned. Retrievable stents are in fact known, but oncethe sleeve has been retracted too far, it is difficult or impossible tocorrect this situation. The advantage of this embodiment of theapplicator according to the first aspect is that stents can thereby bepositioned in a manner which largely permits correction. In any event,the pivotable fingers make it possible, following expansion of thestent, for the stent to be compressed once more and for the stent to beentirely removed or repositioned. In addition thereto, but also entirelyseparately therefrom, the pivotable fingers enable the stent expansionto be carried out in an extensively and particularly controlled manner.

According to a further embodiment of the first aspect, the free, secondfinger ends of the first plurality of fingers are provided with a hookwith a hook opening which opens in the direction of the first fingerends. In the case of a tubular or annular prosthesis, it is thereforepossible to push the fingers through the prosthesis and grip them firmlyfrom the inside by means of the hook opening. This is, for example, analternative to the fingers overlapping the prosthesis from the outside.

According to a further embodiment of the first aspect, the plurality offingers may comprise a second plurality of fingers, the first fingerends of which face towards the proximal end of the instrument and thesecond finger ends face towards the distal end of the instrument. It isnoted here that the term ‘second plurality of fingers’ does not meanthat there must also be a first plurality of fingers. The term ‘secondplurality of fingers’ is used here to make a distinction in relation tothe first plurality of fingers. In this embodiment with a secondplurality of fingers, the instrument may optionally comprise a thirdrod, which extends along the first rod. This third rod will be presentin particular if, in addition to the second plurality of fingers, afirst plurality of fingers as discussed above is also provided, ifrequired, in order to be able to displace the second plurality offingers independently from the first plurality of fingers. In the caseof an aforementioned second plurality of fingers, the fingers of thissecond plurality of fingers, in the absence of an aforementioned firstplurality of fingers, will be displaceable by moving the first rod inrelation to the second rod. In the case where an aforementioned firstplurality of fingers is provided in addition to a second plurality offingers, the fingers of the second plurality of fingers will bedisplaceable by moving the first rod in relation to the second rodand/or by moving the first rod in relation to the third rod, if present.

An embodiment with both an aforementioned first plurality of fingers andan aforementioned second plurality of fingers will be referred to belowas an embodiment with a ‘double head’ or a ‘double-headed’ embodiment.The first plurality of fingers is then associated with a first head andthe second plurality of fingers is then associated with a second head,hence the term ‘double head’. If the medical instrument is used as anapplicator for a prosthesis, it is thus possible to grip the prosthesisfrom two sides. The prosthesis may then possibly be held in place fromone side by one of the two pluralities of fingers, while the other ofthe two pluralities of fingers is then used on the other side of theprosthesis also to hold the prosthesis in place there or otherwise tomanipulate it or to work on the tissue on the other side of theprosthesis. However, a medical instrument according to this embodimentis also usable for purposes other than as an applicator for aprosthesis. The first and second plurality of fingers may, for example,work on a passage from two sides. In the case where the passage is ablood vessel, an obstruction located therein may, for example, be workedon from two sides. However, it is therefore also possible, in the caseof an intervention on a heart valve, to work on the heart valve itselfand/or the area around this heart valve from two sides.

Assuming that, in the embodiment with a double head, the first pluralityof fingers, from the perspective of the operator, is located distallyfrom the second plurality of fingers, the first plurality of fingers canalso be referred to as the distal plurality of fingers, and the secondplurality of fingers as the proximal plurality of fingers.

As stated above, according to the first aspect, in the case of adouble-headed embodiment, the plurality of fingers of the one head maybe provided as mirrored in relation to the plurality of fingers of theother head. In this case, the term ‘mirrored double head’ can be used.However, the plurality of fingers of the one head may, according to thefirst aspect, also be oriented in the same manner as the plurality offingers of the other head (i.e. the first finger ends of the one headand the first finger ends of the other head point in the samedirection). It is also possible, according to the first aspect, for morethan two heads, such as three or four heads, to be provided, with aplurality of fingers for each head.

In the embodiment of the first aspect with a second plurality offingers, the distance from the free ends of the fingers of the secondplurality of fingers to the longitudinal centre line in the firstposition may be greater than in the second position.

According to a further embodiment of the first aspect with a secondplurality of fingers, in the second position, the largest diameterdefined by the second plurality of fingers is smaller than the internaldiameter of the prosthesis, in particular smaller than the internaldiameter which the prosthesis has after it has been detached from theinstrument. This, on the one hand, makes it possible for the secondplurality of fingers, following the detachment of the prosthesis, alsoto pass through the prosthesis and, on the other hand, it can also beensured that the medical instrument, following the detachment of theprosthesis, can easily be retracted from the patient. In any event, theroute that will be taken by the medical instrument and the double headthereof will, in principle, be the same as the route via which theprosthesis is thereby brought to its intended location. If the diameterof the head determined by the second plurality of fingers, following thedetachment of the prosthesis, is less than the internal diameter of theprosthesis, a simple retraction from the access path to the interventionlocation, and/or from the organ and/or the patient, is ensured.

According to a further embodiment of the first aspect with a secondplurality of fingers, the optionally provided third rod is displaceablein relation to the first rod in the longitudinal direction of thelongitudinal centre line for the purpose of operating the fingers of thesecond plurality of fingers. The third rod may be displaceable here inthe proximal direction in relation to the first rod, and/or, conversely,in the distal direction in relation to the first rod.

According to a further embodiment of the first aspect with a secondplurality of fingers, the fingers of the second plurality of fingers,viewed from the first finger end to the free, second finger end, arekinked in a second curved zone in a radially inward direction, whereinthis second curved zone is, in particular, such that the part of thefingers of the second plurality of fingers which is located on the sideof the second curved zone facing towards the second finger end, canextend parallel to the longitudinal direction of the instrument,whereas, viewed from the first finger ends of the second plurality offingers in the direction of the second curved zone, the part of thefingers of the second plurality of fingers located on the side of thesecond curved zone facing towards the first finger ends protrudes in aradially outward direction. A large span, on the one hand, and, on theother hand, a firm grip on a prosthesis or a grip over a long surfacesector on the inner wall of a passage to be worked on can therefore beimplemented with the second plurality of fingers. Due to the partextending parallel to the longitudinal direction of the instrument whichis formed by the part from the second curved zone to the second fingerend, this embodiment is very suitable, in particular, for implanting astent. According to the prior art, it is customary for stents to bedelivered in a sleeve to the intervention location. The sleeve is thenretracted in situ and the stent expands. If the stent is not positionedat precisely the correct location and the sleeve has already beenretracted (too far), the stent can then no longer be repositioned.Retrievable stents are in fact known, but once the sleeve has beenretracted too far, it is difficult or impossible to correct thissituation. The advantage of this embodiment of the applicator accordingto the first aspect is that stents can thereby be positioned in a mannerwhich largely permits correction. In any event, the pivotable fingersmake it possible, following expansion of the stent, for the stent to becompressed once more and for the stent to be entirely removed orrepositioned. In addition thereto, but also entirely separatelytherefrom, the pivotable fingers enable the stent expansion to becarried out in an extensively and particularly controlled manner.

According to a further embodiment of the first aspect with a secondplurality of fingers, the free, second finger ends of the secondplurality of fingers are provided with a hook with a hook opening whichopens in the direction of the first finger ends thereof.

According to a further embodiment of the first aspect, the plurality offingers may comprise a third plurality of fingers, the first finger endsof which face towards the proximal end of the instrument, and the secondfinger ends face towards the distal end of the instrument; and whereinthe distance from the free ends of the fingers of the third plurality offingers to the longitudinal centre line in the first position is greaterthan in the second position. It is noted here that the term ‘thirdplurality of fingers’ does not mean that there must also be a secondplurality of fingers or a first plurality of fingers. The term ‘thirdplurality of fingers’ is used here to make a distinction in relation tothe first and second plurality of fingers. The so-called third pluralityof fingers will, in principle, not be used in combination with the firstplurality of fingers, but it is nevertheless optionally possible for thethird plurality of fingers to be used in combination with the secondplurality of fingers and/or in combination with the first plurality offingers. A double-headed embodiment is also involved in the case of thethird plurality of fingers in the presence of an aforementioned first orsecond plurality of fingers.

According to a further embodiment of the first aspect with a thirdplurality of fingers, in the second position, the largest diameterdefined by the third plurality of fingers is smaller than the internaldiameter of the prosthesis, in particular smaller than the internaldiameter which the prosthesis has after it has been detached from theinstrument. It is thus ensured, following the detachment of theprosthesis, that an instrument with a third plurality of fingers caneasily be retracted through the prosthesis. It is furthermore ensuredthat, even if the medical instrument here is not an applicator for aprosthesis, the medical instrument can be retracted following theintervention along the path via which it was first delivered to theintervention location.

According to a further embodiment of the first aspect with a thirdplurality of fingers, the second rod is displaceable in relation to thefirst rod in the longitudinal direction of the longitudinal centre linefor the purpose of the aforementioned operation of the fingers of thethird plurality of fingers. This displacement in the longitudinaldirection of the longitudinal centre line may be a displacement of thesecond rod in the distal direction in relation to the first rod and/or adisplacement of the second rod in the proximal direction in relation tothe first rod.

According to a further embodiment of the first aspect with a thirdplurality of fingers, the fingers of the third plurality of fingers,viewed from the first finger end to the second finger end, are kinked ina first curved zone in a radially outward direction. The area is thusincreased in span.

According to a further embodiment of the first aspect with a thirdplurality of fingers, the free, second finger ends of the thirdplurality of fingers are provided with a hook with a hook opening whichopens in the proximal direction, i.e. in the direction of the firstfinger ends. Thus, the fingers of the third plurality of fingers, in thecase of a prosthesis, can reach from the proximal side of the prosthesis(facing towards the operator) inside through the prosthesis to thedistal side of the prosthesis (facing away from the operator) in orderto be able to grip there on the prosthesis from the inside by means ofthe hook.

According to a further embodiment of the first aspect with a thirdplurality of fingers, the fingers of the third plurality of fingers,viewed from the first finger end to the free, second finger end, arekinked in a second curved zone in a radially inward direction, and thissecond curved zone is, in particular, such that the part of the fingersof the third plurality of fingers which is located on the side of thissecond curved zone facing away from the first finger ends, can extendparallel to the longitudinal direction of the instrument, whereas,viewed from the first finger end of the third plurality of fingers inthe direction of the second curved zone, the part of the fingers of thethird plurality of fingers which is located on the side of the secondfinger ends adjacent to the second curved zone, protrudes in a radiallyoutward direction. It can thus be achieved that the fingers may, on theone hand, have a relatively long length in the longitudinal direction ofthe instrument, and, on the other hand, for a relatively large part,i.e. up to the first curved zone, can be designed with limiteddimensions, viewed in a radial direction.

According to a further embodiment of the first aspect, the instrument issterile. The term ‘sterile’ is understood here to mean a degree ofsterility which is customary for medical instruments.

According to a further embodiment of the first aspect, the instrumentaccording to the first aspect is made from one or more medicallyacceptable materials. The term ‘medically acceptable materials’ isunderstood to mean materials which, as is customary in the case ofmedical instruments, are inert in relation to, in particular, the humanbody, but usually the animal body also. Examples of medically acceptablematerials of this type include metals such as stainless steel, titanium,nitinol, and plastics such as polypropylene, nylon and Teflon.

According to a further embodiment of the first aspect, the first rod isprovided with a carrier part to carry a prosthesis, and the fingers ofthe at least one plurality of fingers are movable in relation to thecarrier part. Here, the fingers will, in particular, be movable in thedirection of the longitudinal centre line of the medical instrumentand/or in the direction perpendicular to the longitudinal centre line.

According to a further embodiment of the first aspect, the instrument isintended for the implantation of a prosthesis.

According to a further embodiment of the first aspect, the medicalinstrument further comprises a prosthesis, wherein the free ends of thefingers in the one of the aforementioned first and second positions gripon the prosthesis and, in the other of the aforementioned first andsecond positions, preferably lie free from the prosthesis.

According to a further embodiment of the first aspect, the prosthesishas a tubular element, i.e. a hollow element which is open at twoopposite axial ends. This is not yet entirely the same as a so-called‘prosthesis of the type with a tubular element’. The distal and/orproximal flange and distal and/or proximal flange feet may be absent.Apart from a so-called ‘prosthesis of the type with a tubular element’,the prosthesis here may therefore also be a different prosthesis with atubular element, such as a generally known stent.

According to a further embodiment of the first aspect, the ‘prosthesisof the type with a tubular element’ has a distal and proximal flangewhich extend along the circumference of the tubular element, wherein thedistal and/or proximal flange has flange feet which are bendable from anextended position extending in an axial direction to a radial positionextending in a radial direction. In other words, the prosthesis is, inparticular, a prosthesis as described in detail in earlier PCTapplications of the inventor, i.e. WO 00/24339, WO 00/44311, WO03/003926, WO 03/082121 and WO 2005/092246. These PCT applications areall included by reference in the present application as far as detailsof the ‘prosthesis of the type with a tubular element’ are concerned.

According to a further embodiment of the first aspect with a carrierpart, the carrier part is designed to grip on the inside of the tubularelement or organ. A tubular element or organ can thus be supported onthe carrier part, as a result of which the positioning of the tubularelement or organ in relation to the medical instrument, and thereforemore accurate delivery to the intervention location, are moreeffectively ensured.

According to a further embodiment of the first aspect with a prosthesisloaded thereon, biological tissue is located between the prosthesis andthe instrument.

According to a further embodiment of the first aspect, the prosthesis isa heart prosthesis, such as a heart valve prosthesis or ring prosthesis.

According to another further embodiment of the first aspect, theprosthesis is one from the group of:

-   -   the new and inventive ring prosthesis to be described in detail        below (second aspect); and/or    -   the new and inventive stent to be described below (third        aspect).        Second Aspect

According to a second aspect, the present application relates to a newand inventive ring prosthesis. Ring prostheses are prostheses which areused to constrict the through-flow passage of a heart valve or naturalor artificially disposed passages in tissue. According to the secondaspect, a ring prosthesis of this type can also be used in combinationwith an artificial or donor heart valve to draw the surrounding tissuefirmly against the outer circumference of the new heart valve andtherefore prevent leakage around the heart valve. The constricting ringprosthesis can first be disposed here in the tissue and the valveprosthesis can then be placed in or over it. It is advantageous here ifthe ring prosthesis, despite its constricting effect, can then still bewidened so that it can still be stretched to some extent by the valveprosthesis and the valve prosthesis can pass through it. The ringprosthesis may also be integrated, as it were, in advance with the valveprosthesis. The ring prosthesis may then be located here, for example,on the underside or on the upper side of a fixed proximal flange of aprosthesis of the type with a tubular element. A ring prosthesis of thistype may be connected here to the valve prosthesis with adhesions, butthe upper flange of a valve prosthesis of this type may also, forexample, have radially running openings or guide rods which guide thering prosthesis in the radial movements of the ring prosthesis. However,the upper flange of a valve prosthesis of this type may also bedesigned, as it were, as double-walled with radially running openings onthe underside of an upper flange of this type, wherein the ringprosthesis is located inside this upper flange and the pins of the ringprosthesis which are described below project distally through theseradially running openings. Prior to the implanting of a heart valveprosthesis of this type, the distal flange feet of the heart valveprosthesis would first be extended and the diameter of the internal ringprosthesis would be stretched, and possibly the feet thereof would beextended in an axial direction and temporarily held in that condition,so that, following the implantation of the combined product, the distalflange feet of the heart valve prosthesis extend radially, and thediameter of the ring prosthesis has decreased, and the feet of the ringprosthesis have possibly assumed a non-axial direction. It is thusachieved that the tissue around the valve prosthesis is drawn towardsthe valve, and the risk of leakage around the valve is reduced.Separately from the ring prosthesis, the same effect can be achieved byfixing or positioning on or in the upper flange separate pins or pinsinterconnected in a manner other than the manner described here for thering prosthesis, said pins essentially comprising a horizontal part anda vertical part (the actual pin), and wherein the horizontal part can bedisplaced in a resilient manner in a radial direction, wherein thispart, prior to insertion, is stretched in a radially outward directionin order to allow the horizontal part to shorten in a resilient mannerin a radially inward direction following the insertion of the verticalpart, the actual pin itself, into the tissue. The pins must then be heldtemporarily in a mechanical manner by an obstacle in the radiallyoutward position, after which, following removal of this obstacle, whichmay very well be one of the applicators described in this application,the pins move, or at least are inclined to move, radially inwards. Thehorizontal part of pins of this type would then have to be connecteddirectly and in a radial direction to the upper flange, and theresilience could be created by designing the horizontal part as a springor in an waved or zigzag form or otherwise in a resilient manner.

According to the second aspect, the ring prosthesis for constricting thethrough-flow passage of a heart valve comprises:

-   -   a first ring; and    -   anchoring elements to attach the first ring to tissue        surrounding the through-flow passage to be constricted, wherein        each anchoring element is attached to the first ring;        wherein the first ring is formed from a wire which, viewed in        the circumferential direction of the first ring, extends along a        waved pattern in such a way that the diameter of the ring        prosthesis is constrictable from a first, relatively wider,        condition to a second, relatively narrower, condition, wherein        the wave lengths of the waves of the wave pattern in the        aforementioned first condition are greater than in the        aforementioned second condition. The ring prosthesis according        to the second aspect is based on the principle that the        circumference, and therefore the diameter, of the waved ring can        be constricted by drawing the waves closer together, viewed in        the circumferential direction of the ring, i.e. in the extension        direction of the waves. Successive peaks and troughs of the        waves therefore then move closer together. Narrowing of the ring        prosthesis will therefore be accompanied by a reduction in the        wave length and an increase in the wave height, whereas widening        of the ring prosthesis will be accompanied by an increase in the        wave length and a reduction in the wave height.

The advantage of the waved pattern is that a ring prosthesis of thistype according to the second aspect, once it has been implanted, mayfluctuate in diameter to some extent in order to be able to move inconjunction with (pressure) pulses which occur as a result of the effectof the heart, as a result of which the passages through which the bloodis pumped have a tendency to fluctuate in diameter. Furthermore, thewaved pattern also enables the ring prosthesis, if it appears to beslightly too small at the intervention location, first to be widenedbefore it is attached to the surrounding tissue for constrictionthereof.

According to the second aspect, the waved pattern therefore forms acontinuous curve, i.e. the wire extends along a continuous curved pathor, in other words, the wire forms a continuous curved path. The term‘continuous curve’ is understood here to mean a curve of which the(mathematical) direction coefficient runs gradually, as in the case, forexample, of a parabola or sinusoidal form. Abrupt transitions, as aresult of which the wire would be susceptible to breaking, are thusavoided.

The anchoring elements in a ring prosthesis according to the secondaspect can be designed in many different ways. If a suture is used tosew surrounding tissue, for example, to the peaks of the waves, thesuture will form the anchoring elements and the ring can therefore evenbe delivered without anchoring elements having been previously attachedthereto. The anchoring elements may also comprise clamps, consisting,for example, of a so-called lower and upper flange as described in theaforementioned PCT applications of the inventor, i.e. WO 00/24339, WO00/443111, WO 03/003926, WO 03/082121 and WO 2005/092246.

According to a further embodiment of the second aspect, the waved wireis in the first condition and the ring, in this first condition, isunder a pre-tension, as a result of which the ring is inclined toconstrict to the second condition. The ring is then fixed here in thefirst condition and, once the fixing has been undone, will be inclinedto move towards the second condition under the influence of thepre-tension. This can be implemented, for example by designing the wirein the form of a memory material, such as a memory metal. An example ofa memory metal of this type is a nitinol alloy. If the ring is made froma nitinol alloy (or other memory metal), the ring can be ‘frozen’ bymeans of a temperature treatment, in particular a cold treatment, in thewide first condition. The ring can then be heated and, when a thresholdtemperature is exceeded, the ‘frozen’ pre-tension will be released, sothat the ring can return to the narrower second condition. A differentway of implementing a ring pre-tensioned in the wider first condition isto design said ring from a ‘normal’ resilient, elastic material (such asa spring-steel-type material), and then to stretch the ring, while thepre-tension is built up here, to the first condition and fix it by meansof (mechanical) obstacles in this first condition. When the mechanicalobstacle is removed, the pre-tension is then released and the ring willbe inclined to return to the narrower, second condition. Combinations ofpre-tension created with temperature treatment of memory material and atemporary mechanical obstacle are of course also possible.

According to a further embodiment of the second aspect, the anchoringelements comprise pins. These pins are attached at one end to the ringprosthesis and, viewed from this one end, may extend in particular inthe axial direction of the first ring. This makes it possible to pressthe pins into the natural annulus around a heart valve and therebyattach the ring prosthesis. The ring prosthesis can then be constricted.

According to the second aspect, the constriction of the ring prosthesismay be effected by exerting mechanical force upon it. It is also veryeasily conceivable for the ring prosthesis, in particular the waved wirethereof, to be made from a memory material, such as a memory metal (forexample a nitinol alloy) or a memory plastic, such as a polymer withmemory properties. A ring prosthesis of this type, once it has beenattached and has reached body temperature or has possibly been heated toa slightly higher temperature, can then return to an original narrowerdiameter which is, as it were, stored in the memory of the memorymaterial.

According to a further embodiment of the second aspect with pins, atleast a part of the pins is pre-tensioned in order to move the freeends, once the pre-tension has been released, in relation to the ends ofthe pins attached to the ring prosthesis. All pins can therefore also bepre-tensioned here. This pre-tensioned condition is maintainable, forexample, with the aid of a mechanical obstacle which is removed when thering prosthesis is implanted. However, this pre-tension can also beimplemented by means of a memory material, wherein the pins are then‘frozen’ in the axial condition, normally by means of a temperaturetreatment. If a specific threshold temperature is exceeded, the pinswill then be inclined to return to a condition in which the free endsare displaced in relation to the ends attached to the ring prosthesis.The anchoring in surrounding tissue can be improved by displacing thefree ends of one or more of the pins in relation to the ends of the pinsattached to the ring prosthesis. The movement of the free ends of thepins in relation to the ends attached to the ring prosthesis can beimplemented by positioning the pins, wherein their shape does notchange, obliquely or more obliquely in relation to the axial directionof the ring prosthesis and/or by bending the pins.

According to a further embodiment of the second aspect, the pins, or atleast a part thereof, are pre-tensioned in order, following release withthe free ends, to:

-   -   to be displaced in a radially inward direction; and/or    -   to be displaced in a radially outward direction; and/or    -   to be displaced in a tangential direction; and/or    -   to be displaced in pairs towards one another.        The term ‘displaced in pairs towards one another’ is understood        here to mean that the free ends of two pins move towards one        another and possibly thereby cross one another. Two such pins        therefore form a type of anchoring clamp. The radial        displacement of the free ends of the pins may even take place to        the extent that the pins, as it were, curl up over 90° or even        more, up to 180°. It will be clear that this improves the        anchoring of the pins in the surrounding tissue.

According to a further embodiment of the second aspect, the anchoringelements are disposed in a distributed manner, in particular evenlydistributed, over the circumference of the first ring.

According to a further embodiment of the second aspect, the ringprosthesis further comprises a plurality of segments disposed in adistributed manner over the circumference of the first ring, whereineach segment is attached to the first ring. According to a furtherdesign thereof, segments adjacent in the circumferential direction may,in the first condition, lie at a distance from one another leaving theintermediate space free, and, in the second condition, lying against oneanother, may form an essentially closed second ring which preventsfurther constriction. It can thus be achieved that the constriction ofthe ring prosthesis is limited to a predefined diameter. The ringsegments may therefore have a limiting function. An entirely differentfunction of the ring segments is a support/attachment function. Inaddition to or entirely separately from the limiting function, the ringsegments may also serve to support a further prosthesis which is to beimplanted in or near the ring prosthesis and/or to affix a furtherprosthesis of this type. In the case of this support/attachmentfunction, it is also possible for only a few, at least 2 or 3, ringsegments to be provided, which are distributed over the innercircumference of the waved wire ring and which together cannot form acomplete ring. The ring segments do not therefore have to be able toform a closed ring for the support/attachment function. There do noteven have to be any ring segments.

According to a further embodiment of the second aspect, the amplitude ofthe waved pattern extends in the radial direction of the ring. Inparticular, the amplitude of the waved pattern extends here at an angleof 30° to 90° in relation to the axial direction of the first ring. Thering prosthesis, following implantation, may therefore lie close toannulus tissue or other tissue oriented radially in relation to the ringprosthesis.

According to a further embodiment of the second aspect, the position ofthe amplitude of the waved pattern, viewed along the circumference ofthe first ring, varies in relation to the axial direction of the firstring. Thus, if the ring is used in the case of the mitral valve, it maybe advantageous, for example, if the position of the amplitude isdesigned over a ⅓ or ¼ part of the ring with an angle which is narrowerin relation to the axial direction than in the case of the remainder ofthe ring, said part lying on the anterior or septal side of the mitralannulus.

According to a further embodiment of the second aspect, the ringprosthesis comprises at most one aforementioned anchoring element foreach cycle of the waved pattern. It can thus be achieved that anchoringelements adjacent in the circumferential direction cannot obstruct oneanother. The anchoring elements can be attached here in each case to thefirst ring in the same part of the cycle of the waved pattern.

According to a further embodiment of the second aspect with oneanchoring element for each wave cycle, the anchoring elements areattached to the inward-facing troughs of the waved pattern, inparticular at the midpoint of said troughs. The anchoring elements heremay, for example, be pins or clamping mouths, as will be discussedbelow. If the anchoring elements are located in the trough of the waves,the implementation may be such that, insofar as possible, followingimplantation, the entire ring prosthesis, and therefore the materialthereof which is foreign to the body, is located outside the valvepassage.

It is noted that the anchoring elements may also be provided between thepeaks and troughs, for example midway between the peaks and troughs.

According to a further embodiment of the second aspect, in each casewith one anchoring element for each cycle, the anchoring elements areattached to the outward-facing peaks of the waved pattern, in particularat the midpoint of said peaks. The anchoring elements here may be thepins discussed earlier.

According to a further embodiment of the second aspect, the wavedpattern is a sinusoidal pattern. The term ‘sinusoidal pattern’ isunderstood in particular to mean a pattern which runs along a line witha curve continuously changing according to a sine-wave pattern. Sharplyangled parts which form a thrombosis in contact with blood or canotherwise cause disruption to the blood flow are largely avoided here. Asinusoidal waved pattern enables an effectively controllable narrowingof the diameter. Furthermore, a sinusoidal waved pattern enables aflexible small diameter adaptation in response to pressure fluctuationsin the bloodstream, or the cyclical heart muscle action.

According to a further embodiment of the second aspect, the wavedpattern comprises 8, 9, 10, 11, 12, 13, 14 or 15 wave cycles, whereinthe first ring has a diameter in the 15 mm to 50 mm range. The diameterhere is in particular related to the diameter of the ring prosthesis asthe latter is delivered ex-works. The ring prosthesis may be deliveredex-works in an expanded condition in order to narrow followingimplantation. However, the ring prosthesis may also be deliveredex-works in a constricted condition, wherein the operator will thenwiden the ring prosthesis prior to or during implantation, for exampleby cooling it by placing it on a cooled holder or by placing it in icewater and actively stretching it, in order to allow the ring prosthesisto narrow once more following implantation, for example through contactwith the warm body tissue or blood, or by actively heating it with awarm holder, or with a warm liquid. For an application of the ringprosthesis according to the second aspect in the case of a mitral ortricuspid valve, the diameter will normally lie in the 25 to 40 mmrange. In the case of aortic valves, the required diameters for the ringprosthesis will lie, in particular, in the 17 mm to 29 mm range. If thering prosthesis is used to constrict natural or artificially disposedpassages elsewhere in the body, the diameters may be larger or smaller.For use in the case of an aortic valve, the ring prosthesis according tothe second aspect may also have, along with the waved pattern, i.e.superimposed thereon, a sinusoidal form of 3 sine waves in thecircumferential direction.

According to a further embodiment of the second aspect, viewed in thedirection of the wave height, the distance between the peaks and troughsof the waves lies in the 0.5 mm to 20 mm range, such as in the 0.5 to 3mm range. Ring prostheses with such dimensions for the wave pattern canbe used in humans for virtually any type of heart valve.

The diameter of the first ring, the wave height and the number of wavecycles may vary according to the type of heart valve and according tothe patient.

According to a further embodiment of the second aspect, the anchoringelements may comprise clamping mouths with a first jaw part and a secondjaw part which is movable in relation to the first jaw part in order toclamp tissue between the jaw parts. Clamping mouths of this type areknown per se from the aforementioned PCT applications (i.e. WO 00/24339,WO 00/443111, WO 03/003926, WO 03/082121 and WO 2005/092246 of theinventor), and are normally referred to in said applications by the term‘lower and upper flange feet’.

According to a further embodiment of the second aspect with clampingmouths, the clamping mouths can be brought from a closed conditionagainst spring action to an open condition, and the clamping mouths canbe returned from the opened condition to the closed condition under theinfluence of said spring action. The spring action may be provided hereby means of a conventional mechanical spring action. However, the springaction may also be provided by using memory material. According to afurther embodiment, the clamping mouths then also comprise a memorymaterial which produces said spring effect, wherein the clamping mouthsare fixed in the opened condition by means of a temperature treatment(which is understood in all aspects of this application to mean not onlya treatment at a higher temperature, also referred to as heat treatment,but also a treatment at a lower temperature, also referred to as coldtreatment) in order to be able to return to the closed condition if athreshold temperature is exceeded or understepped. The memory materialhere may be a memory metal, such as nitinol, but may also be a memoryplastic, such as a memory polymer. Combinations of memory metal andmemory plastic are also conceivable. In the case of nitinol, theclamping mouths may be fixed in the opened condition by means of a coldtreatment, in order to return later to the closed condition if they warmup and exceed the threshold temperature.

According to a further embodiment of the second aspect with clampingmouths, the clamping mouths are provided on the inner circumference orouter circumference of the ring prosthesis and are pointed with themouth opening in a radially outward direction. If the clamping mouthsare provided on the inner circumference and are oriented with the mouthopening in a radially outward direction, it is optionally possible todesign the ring prosthesis in such a way that, viewed in the axialdirection, the clamping mouths are essentially entirely overlapped by asurface which is defined, on the one hand, by the inner contour of thewire determined by the wave troughs and, on the other hand, the outercontour of the wire determined by the wave peaks.

According to a further embodiment of the second aspect, the clampingmouths comprise one or more teeth which are attached, in particular, toa jaw part and point towards the opposite jaw part. The adhesive forceon the tissue clamped in the clamping mouths can thus be increased.

The basic shape in the case of a ring prosthesis according to the secondaspect is determined by an imaginary line which interconnects the wavepeaks. Alternatively, but essentially equivalent, this basic shape canalso be determined by an imaginary line which interconnects the wavetroughs, or the imaginary line which forms the midpoint between the wavetroughs and wave peaks. On the basis of this basic shape definition, itis noted that the basic shape of the ring prosthesis according to thesecond aspect may be adapted to the shape of the relevant heart valvewhere it will be used. The basic shape does not therefore have to be acircular shape, and the designations ring prosthesis, first ring andsecond ring do not then suggest a circular shape either (although acircular shape is not excluded). The basic shape may also be anelliptical, bean, kidney or other shape. The basic shape may even benon-symmetrical. Where the diameter of the ring prosthesis is mentionedabove, this is not therefore intended to mean that the ring prosthesismust be circular, but is intended to designate a dimension across theaxial direction of the ring prosthesis. As far as the basic shapes forring prostheses according to the second aspect are concerned, it ispointed out in particular that they may be bean-shaped, for use, inparticular, in the case of a mitral or tricuspid valve. It isfurthermore pointed out that the basic shape does not have to be2-dimensional, but may also be a 3-dimensional shape. For example, inthe case of an aortic valve, the natural annulus runs, for example,according to a sinusoidal pattern of 3 sine waves. Correspondingly, thebasic shape for a ring prosthesis according to the second aspect whichis intended for an aortic valve may follow a sinusoidal pattern, such asa sinusoidal pattern with 3 sine waves. This sinusoidal pattern extends,on the one hand, where the propagation direction of the sine wave isconcerned, along the circumference of the ring prosthesis and, on theother hand, where the amplitude direction of the sine wave is concerned,in the axial direction of the ring prosthesis. An example of a furtherexplanation of a sine-wave pattern of this type can be found in WO00/44311 of the inventor, in particular in FIG. 7 of WO 00/44311 and inthe description associated with FIG. 7 of WO 00/44311.

Third Aspect

According to a third aspect,

this application also relates to a new and inventive stent.

A stent is a tube, normally made of metal, with an open grid structure,often with a cylindrical shape, which is compressible, and, if held inthe compressed condition, often by means of a mechanical obstacle, suchas a tube or a sleeve, can be navigated to a required intended locationin the body of a patient. Once the stent has reached the intendedlocation, the stent can be released by removing the tube or sleeve,after which the stent will open out through radial expansion, and can beaffixed against the wall of a cylindrical channel, such as e.g. a bloodvessel. If a stent is then used to affix a heart prosthesis, referred toas a valved stent, the following problems arise. The first problem isthat, at places where a natural heart valve is located in the heart,this place and the immediate surroundings thereof are not always purelycylindrical in shape, or are even on the whole non-cylindrical in shape.The second problem is that a heart valve prosthesis has a specificoptimum diameter, so that deviation therefrom is not possible if anoptimum result is to be achieved.

The first problem may mean that the stent is poorly affixed in situ. Inthe case of the aortic valve and the pulmonary valve, this is not aproblem, seeing that these valves are located on the underside ofessentially cylindrical channels, i.e. the aorta and the pulmonaryartery respectively. However, in the case of the mitral valve and thetricuspid valve, these valves are, on the whole, not located in acylindrical channel, but between two relatively wide spaces, i.e.,respectively in the case of the mitral valve, between the left atriumand the left ventricle, and, in the case of the tricuspid valve, betweenthe right atrium and the right ventricle. A cylindrical stent cannot beaffixed or cannot be firmly affixed there. To counteract this, it isknown from the current prior art that a stent can also widen or narrow.For example, in the case of an aortic valved stent, the stent can bewidened on the upper side (downstream), so that the stent can be affixedat a distance from the original aortic valve, i.e. in the ascendingaorta. If an affixing at a distance of this type were to be used in thecase of the atrioventricular valves, this would then require not only alarge amount of stent material, but also a stent with a large diameter.Material of this type would act as an obstruction to the blood flow ofthe chambers and the atria. The atrial tissue is very thin and willoffer little resistance to the stent, and could easily be perforated bythe stent. Furthermore, the anatomy of the atria is subject to greatvariation. Such broadenings of the stent at a distance from the valveannulus do not result in a mechanically effective adhesion, compressionor hooking in the region of the valve annulus, and cannot preventleakage around the stent in the region of the annulus.

As mentioned, the second problem is that a heart valve has a specificoptimum diameter. A mechanical heart valve prosthesis has a fixeddiameter. A biological heart valve prosthesis comprises valve flaps andis deformable, possibly also compressible and expandable, and has anoptimum diameter, wherein the passage for blood is optimum. If the valvediameter is overstretched, this may result in damage to the valve flaps,or even incomplete closure of the valve flaps. If the biological heartvalve prosthesis is not fully expanded, the valve flaps may act as anobstruction to the blood flow, or the shape of the valve flaps may bedeformed, or blood turbulence may occur, which may result in reduceddurability of the valve. It is therefore important for a possible firstcompressed biological valve prosthesis to be expanded duringimplantation in such a way that the valve obtains its optimum diameter.If such a valve is then fixed in a stent, in most cases throughadhesions, or otherwise, it is then clear that, at the time when thebiological valve prosthesis has attained its optimum diameter, it cannotfurther expand, as a result of which the radial expansion forces of thestent at that moment are reduced to virtually zero. At any rate, thevalve then retains the stent. In other words, the adhesive force of thestent is virtually zero at the time when the valve is fully expanded. Toavoid this problem, it is generally advised to use a slightly largervalve (and stent) diameter than would be strictly necessary, with all ofthe aforementioned disadvantages as far as the incomplete opening ordeformed shape of the valve flaps is concerned. An alternative is to usea wider stent, which is affixed at a distance from the valve annulus.Furthermore, the current aortic valved stents are used in practice incombination with a balloon dilatation of often calcified diseased aorticvalves, so that the valve and stent are affixed in the dilated andcalcified diseased valve, wherein the stent hooks onto the calcareousdiseased valve tissue. If, in the case of a diseased valve, the diseasedvalve is entirely removed, the valved stent will only be able to beaffixed if a diameter is used which is actually too large, or if theattachment actually takes place at a location other than in the regionof the valve annulus.

According to the third aspect, the object of this application is toovercome one or more of the aforementioned problems relating to stents.

This object is achieved according to the third aspect by providing astent, comprising:

-   -   a tubular element which is expandable in a radial direction from        a compressed condition to an expanded condition, and which has a        proximal and distal end;    -   a proximal flange of proximal flange feet provided around the        tubular element; and    -   a distal flange of distal flange feet provided around the        tubular element;        wherein the distal and proximal flange feet are attached with a        fixed end to the tubular element and have another end which is        free;        wherein the distal and proximal flange feet have a radial        position, in which the free ends of the flange feet point in the        radial direction for anchoring with surrounding tissue;        wherein the distal flange feet are pivotable from an extended        position, in which the distal flange feet lie in the        longitudinal direction of the tubular element, to the position        extending in the radial direction; and wherein the distal flange        feet are provided distally from the proximal flange feet. As far        as the so-called proximal and distal flange feet are concerned,        it is noted here that they are essentially comparable with        distal and proximal flange feet (or arms) as known from WO        00/24339, WO 00/44311, WO 03/003926, WO 03/082121 and WO        2005/092246. The stent according to the invention is based on        the insight that the knowledge disclosed by the aforementioned        PCT application is also readily applicable to stents in order to        attach the latter to surrounding tissue. The anchoring to        surrounding tissue is carried out here in that surrounding        tissue is clamped between the distal and proximal flange feet        and/or in that the distal and proximal flange feet anchor        themselves in the surrounding tissue as a clamp, in particular        with distal and proximal flange feet pointing towards one        another or crossing one another. The tubular element of the        stent according to the invention will not normally be a solid        element but a grid-like element as is generally known in the        medical field in the case of stents. According to a further        design, the free ends of the distal flange feet, in the extended        position, optionally point in the distal direction.

It is noted that, according to the third aspect, the tubular elementdoes not have to have the same diameter overall. The tubular elementmay, for example, have a first and second zone, wherein the diameter inthe first zone is smaller than in the second zone. The proximal and/ordistal flange may then be provided in the first and/or second zone. Ifthe proximal and/or distal flange are provided in the first zone, wherethe diameter is smaller, it is even conceivable that the circumferentialcontour, defined by the ends of the flange feet in the case of theproximal or distal flange in the radial position, has a diameter whichis smaller than the diameter of the second zone.

In the case of the stent according to the third aspect of thisapplication, the proximal flange feet may also optionally be pivotablefrom an extended position, in which the proximal flange feet lie in thelongitudinal direction of the tubular element, to a radial positionextending in the radial direction. In this design, the free ends of theproximal flange feet, in the extended position, may optionally point inthe proximal direction.

It is noted that the extendable distal flange feet, in the extendedcondition, may also lie along the tubular element and also in theextension of the tubular element if they are provided on one end of thetubular element. The same applies to the proximal flange feet, if theyare extendable. Extendable proximal flange feet may, in the extendedcondition, lie along the tubular element and also in the extension ofthe tubular element, if they are provided on one end of the tubularelement.

By combining the so-called ‘tubular element’ from WO 00/24339, WO00/44311, WO 03/003926, WO 03/082121 and WO 2005/092246 of the inventorwith a stent, wherein the lowermost flange is bendable and the uppermostflange may also optionally be bendable, a so-called valved stent may befirmly and reliably affixed in a mechanical manner in the region of thevalve annulus. The diameter of the expandable tubular element may matchthe optimum diameter of the valve prosthesis. The stent is thenessentially no longer necessary, as is the case in the prior art, inorder to affix the valve prosthesis, but is primarily a tool to hold thebiological valve extended and upright. However, it is possible, in thecase of the stent according to the third aspect of this application, forthe total product of the stent and valve to be compressible andtherefore to be able to be brought more easily to the interventionlocation in the body of the patient.

Other advantages of the stent according to the third aspect of thisapplication compared with the current (aortic) valved stents are that,insofar as the current valved stents make use of stents to affix thestent to the surrounding tissue at a distance from the valve annulus,this increases the quantity of the material foreign to the body and thisstent material may have a thrombogenic effect. Due to the greater lengthof the stent from the prior art, an obstruction to the blood flowthrough the coronary arteries will more readily occur, and it is moredifficult for the surgeon to find space on the ascending aorta forso-called proximal anastomoses with bypass grafts. Problems of this typecan be prevented with the stent according to the third aspect of thisapplication in that it is affixed very locally, preferably in the regionof the valve annulus.

In a further embodiment of the third aspect, the fixed ends of thedistal flange feet are located at a distance from the distal end of thetubular element which is larger than twice the length of the distalflange feet; and the fixed ends of the proximal flange feet are locatedat a distance from the proximal end of the tubular element which isgreater than 2× the length of the proximal flange feet.

In the case of a stent according to the third aspect, the proximal anddistal flange feet interact to clamp or firmly grip surrounding tissuebetween them after they have bent in the direction of the radialposition. It must be noted that the distal and proximal flange feetdefined here do not have to assume a purely radial position, as whatmatters here is that they anchor themselves in the surrounding tissue.It is conceivable here that surrounding tissue holds the flange feetessentially in a largely axial position. The flange feet may possibly beprovided here with hooks or small pins, or may even be designed as hooksfor further anchoring in the surrounding tissue.

According to a further embodiment of the third aspect, the stentcomprises a heart valve provided in the tubular element. This heartvalve may be a natural donor valve, normally referred to by the personskilled in the art as a ‘biological valve’, such as from a human, knownto the person skilled in the art as a ‘homograft’, or animal, known tothe person skilled in the art as a ‘xenograft’. According to a furtherembodiment, the donor valve is a biological valve selected from thegroup of:

-   -   porcine valves, such as a reconstructed or non-reconstructed        aortic valve from a pig, including the three valve flaps;    -   bovine valves, such as a reconstructed or non-reconstructed        valve, for example with three valve flaps reconstructed from the        pericardium of a bovine animal;    -   equine valves;    -   human valves; or    -   kangaroo valves.        None of these biological valves needs to be entirely biological,        but, in addition to biological material, may also comprise        non-biological material such as plastic or metal. Furthermore,        these biological valves may or may not be a reconstructed valve.        A reconstructed valve is generally understood to be a valve of        biological material, from which the original anatomical link has        been broken. A reconstructed valve may be formed by combining a        plurality of biological components into a valve. The plurality        of biological components may originate from the same donor or        from different donors. It is even conceivable for the biological        components to originate from different types of donor, for        example one or more components originating from a pig in        combination with one or more components originating from a        bovine animal, or one or more components originating from a        human in combination with one or more components originating        from different or the same types of animal.

According to a further design of the third aspect, the tubular elementand the distal and proximal flange feet comprise a single piece ofmaterial. The unit may be manufactured, for example, by laser burning oretching from a single piece. This single piece may be a tubular or otherform of a plate of material, for example of metal such as stainlesssteel or a nitinol alloy. The plate material may be in a flat or curvedcondition prior to the formation of the unit and may be closed to atubular form following removal of material, but the plate material mayalso have a tubular configuration prior to the removal of material.Furthermore, it is of course also possible for the tubular element, thedistal flange feet and the proximal flange feet to be assembled fromdifferent components into one unit.

According to a further embodiment of the third aspect, the separateflanges, or parts thereof, or the separate flange feet of the separateflanges have an unequal shape and/or length and/or width in relation toone another, and/or angle in relation to the longitudinal axis, and/orfillings (which will be discussed below in the fourth aspect).

According to a further embodiment of the third aspect, the fillings(which will be discussed below in the fourth aspect) of the separateflanges, or the separate flange feet of the separate flanges have, inrelation to one another, an unequal shape, and/or length, and/or width,and/or angle in relation to the longitudinal axis, and/or consistency,and/or material properties.

According to a further embodiment of the third aspect, the fillings(which will be discussed below in the fourth aspect) of the separateflange feet extend beyond the circumference of a flange foot, and in alateral and/or radial direction therefrom.

According to a further embodiment of the third aspect, the fillings(which will be discussed below in the fourth aspect) of the separateflange feet are interconnected in such a way that a continuity arisesbetween all or a number of fillings of the flange feet of one or bothflanges.

Fourth Aspect

According to a fourth aspect, this application also relates to a new andinventive prosthesis, in particular a ‘prosthesis of the so-called typewith a tubular element’, as described as a vascular prosthesis in WO00/22339 and as a heart prosthesis in sections 1.1, 2.1, 3.1 and 4.1 ofWO 00/44311. WO 00/22339 in its entirety, and WO 00/44311, sections 1.1,2.1, 3.1 and 4.1, are included by reference in this application forfurther details of the prosthesis according to the fourth aspect.

The fourth aspect of this application is also very readily applicable incombination with one or more of the other aspects of this application,such as, inter alia, the third and sixth aspect of this application.

Memory material, such as nitinol, has the favourable property that itcan be deformed from a first condition to a second condition, and can befixed in this second condition. By exceeding or understepping a specificthreshold temperature, the fixing can be undone, after which a reversedeformation from the second condition to the first condition takesplace. However, restrictions apply to this deformation and reversedeformation. If memory metal, such as nitinol, is deformed with anabrupt transition, as in the case of a sharp crease, permanentdeformations occur. As a result of these permanent deformations, thefinal condition remaining after reverse deformation differs from theoriginal first condition. It is even possible that little or nodeformation will take place. The memory then functions, so to speak,less well or not at all. To prevent this, it is customary to avoid sharpbends by using a concave shape, at the location of a sharp bend, so tospeak in the axil thereof, which makes the bend much more gradual. Inthe case of ‘prostheses of the tubular type defined earlier’, a sharpcurve is usually required in the axil, which, as a result of themeasures to cause the bending to run gradually, results in a concavecavity in the axil. This concave cavity reduces the clamping forcerequired for anchoring to the tissue at the location of the axil. Thefourth aspect of this application intends to improve the clamping forcebetween the proximal and distal flange.

This object is achieved according to the fourth aspect by providing aprosthesis for attachment in a passage surrounded by tissue,

wherein the prosthesis comprises a tubular element formed from memorymaterial with a proximal and distal flange which extend around thetubular element;

wherein the distal and proximal flange have a radial position, in whichthey project from the tubular element in a radially outward direction inorder to clamp tissue surrounding the passage between the distal andproximal flange;

wherein the distal flange consists of distal flange feet, which arebendable from the radial position, against a pre-tension created by thememory material, to an extended position, in which the distal flangefeet extend in the longitudinal direction of the tubular element andwhich are fixable in this extended position, in order to return to theradial position under the influence of the pre-tension once the fixinghas been undone;wherein the distal flange feet, at the ends attached to the tubularelement, are provided on the side facing the proximal flange with afilling which is designed, in the radial position of the distal andproximal flange, to increase the clamping force with which the distaland proximal flanges clamp the tissue in situ. The inventor has notedthat the properties of memory material are not readily capable ofproviding a firm clamping force in the vicinity of the ends attached tothe tubular element, but that this clamping force can be considerablyimproved by providing a filling in that area which, in the clampedcondition, is located between the respective flange feet and the tissueto be clamped.

According to a further embodiment of the fourth aspect, the distalflange feet have a concave-curved part which follows on from the ends ofthe distal flange feet attached to the tubular element, wherein thehollow side of the concave-curved part faces towards the proximalflange, and wherein the filling is provided in the hollow side of theconcave-curved part. The inventor has noted that memory material hasparticular difficulty in bending over a sharp curve under the influenceof the memory effect and as a result clamping force is lost. This can beprevented according to the fourth aspect of this application byproviding the concave part with the filling therein.

According to a further design of the fourth aspect with a concave-curvedpart, the filling protrudes from the cavity formed by the concave partin the direction of the opposite flange feet. The clamping effect and/orsealing at the location of the concave-curved part can thus beincreased.

According to a further embodiment of the fourth aspect with a projectingfilling, the filling is compressible in such a way that, if the flangefeet are in the radial position, the part of the filling protruding fromthe cavity can be compressed. The clamping effect and sealing can thusbe even further improved.

According to a further embodiment of the fourth aspect, theconcave-curved part of the distal flange feet, on the side thereoffacing towards the free ends of the distal flange feet, viewed in theradial direction and radial position, changes to a straight part. Thisstraight part preceded by a concave-curved part appears to be capable ofproviding an effective clamping force.

According to a further embodiment of the fourth aspect, the proximalflange can be provided, in a manner corresponding to the distal flange,with proximal flange feet which are bendable from the radial position,against a pre-tension created by the memory material, to an extendedposition, in which the proximal flange feet extend in the longitudinaldirection of the tubular element, and which are fixable in this extendedposition in order to return to the radial position under the influenceof the pre-tension once the fixing has been undone; wherein the proximalflange feet, on the ends attached to the tubular element, on the sidefacing towards the distal flange, are provided with a filling which isdesigned, in the radial position of the distal and proximal flange, toincrease the clamping force with which the distal and proximal flangeclamp the tissue in situ. In a corresponding manner, according to afurther design, the proximal flange feet may have a concave-curved partwhich follows on from the ends of the proximal flange feet attached tothe tubular element, wherein the hollow side of the concave-curved partfaces towards the distal flange, and wherein the filling is provided inthe hollow side of the concave-curved part. Furthermore, in this design,the concave-curved part of the proximal flange feet, on the side thereoffacing towards the free ends of the proximal flange feet, viewed in theradial direction and radial position, may also optionally change into astraight part.

In a further design of the fourth aspect, the filling is made from amaterial other than the material from which the tubular element, thedistal flange and the proximal flange are made. The filling may, forexample, be made or may comprise the same material as the material fromwhich the tubular element is made. However, the filling may also be madefrom or may comprise a synthetic foam or textile, such as thosegenerally used in the medical device industry for various applications,for example Dacron, Teflon and various types of polyester.

In a further design of the fourth aspect, the memory material is amemory metal. The memory metal here may be a nitinol alloy.

Fifth Aspect

According to a fifth aspect, the application relates to a new andinventive applicator for implanting a hollow prosthesis with an opendistal end and an open proximal end.

Examples of hollow prostheses of this type include:

-   -   hollow designs of a ‘prosthesis of the type with a tubular        element’ such as the prosthesis described as a vascular        prosthesis in WO 00/22339 and as a heart prosthesis in sections        1.1, 2.1, 3.1 and 4.1 of WO 00/44311. In this connection, WO        00/22339 in its entirety and WO 00/44311 sections 1.1, 2.1, 3.1        and 4.1 are included by reference in this application for        further details of the prosthesis.    -   stents, such as the stent according to the third aspect of this        application;    -   ring prostheses, such as the ring prosthesis according to the        second aspect of this application or a ring prosthesis as known        from WO 00/44311 and WO 03/082121 of the inventor, which, in        this context, are included by reference in this application for        further details of the prosthesis.        Hollow prostheses of this type are normally intended for        implantation in a passage through which blood or another fluid        flows. The blood or other fluid will then enter and leave the        prosthesis at the opposite open ends.        According to the fifth aspect, the object of the present        application is to provide an applicator for a hollow, distally        and proximally open prosthesis, said applicator being of simple        construction and also being simple and reliable in use.

This object is achieved according to the fifth aspect by providing anapplicator for the implantation of a hollow prosthesis with an opendistal end and an open proximal end, comprising:

-   -   a tube with an inner screw thread over at least a part of the        length thereof;    -   a pin extending through the tube with, over at least a part of        the length thereof, an outer screw thread which mates with the        aforementioned inner screw thread;        wherein the tube carries a sheathing on the distal end thereof;        wherein the pin is equipped, on the distal end thereof, with a        carrier for a prosthesis, said carrier, on the one hand, being        rotatable in relation to the pin around the longitudinal centre        line of the pin and, on the other hand, being shiftable from a        position pushed out from the sheathing in the proximal direction        in relation to the sheathing to a position entirely or partially        retracted into the sheathing, by rotating the tube in relation        to the pin; and        wherein the applicator further comprises an axial guide which is        designed, on the one hand, to prevent rotation of the carrier in        relation to the sheathing around the longitudinal centre line of        the pin and, on the other hand, to allow axial shifting of the        carrier in relation to the sheathing.        The operation of this applicator is very simple and reliable. By        merely rotating the pin in relation to the tube, the pin will be        able to move in the proximal direction in relation to the tube        as a result of the mating inner and outer screw thread. The        carrier, which is mounted on the distal end of the pin, is        pushed into the sheathing, and the prosthesis provided on the        carrier will be held in place by the distal edge of the        sheathing. Thus, viewed in relation to the carrier, the        prosthesis will be pushed away in the distal direction of the        carrier and will be detached. Any hollow, annular or tubular        prosthesis can be simply and reliably implanted with this        applicator. Furthermore, the structural design of this        applicator is simple and robust.

According to a further design of the fifth aspect, the carrier, on thedistal end thereof, comprises a nose part tapering in the distaldirection with a rounded point. The applicator, or at least the distalend thereof, can easily be fed, with a nose part of this type, through achannel or other passage to the intervention location. When used for theimplantation of a ring prosthesis in an atrioventricular valve, thisnose part will have the additional advantage that the valve flapsthemselves are thereby held back and protected from the prosthesis to beimplanted, so that they cannot thereby be damaged.

According to a further design of the fifth aspect, the carrier part hasa carrier surface facing radially outwards, the outer contour of whichmatches the inner contour of the sheathing. The carrier can thus slideinwards into the sheathing essentially without play when the prosthesisis detached. The prosthesis can then no longer slide inwards into thesheathing or be squeezed between the sheathing and the carrier. Areliable and effective detachment of the prosthesis is thus ensured.

According to a further design of the fifth aspect, the tube and the pinare designed to be flexible, such as bendable or kinkable, over at leasta part of the length thereof, in such a way that the longitudinal centreline of the tube and pin is flexible, such as bendable or kinkable. Theapplicator can thus be used in curved access routes. This can beimplemented, inter alia, if the tube and the pin, over at least a partof the length thereof, are designed from superelastic material, such asnitinol designed in superelastic form; and/or if the tube and the pin,over at least a part of the length thereof, are designed as a wire, suchas steel wire.

The fifth aspect further relates to an assembly, comprising, on the onehand, an applicator according to the fifth aspect and, on the otherhand, an aforementioned hollow prosthesis, in particular a heartprosthesis, wherein the prosthesis carried by the carrier is disposed onthe carrier. The prosthesis may be clamped in place on the carriersurface. The clamping may be very light so that, on one hand, it is justsufficient to prevent the prosthesis from sliding prematurely off thecarrier and, on the other hand, the clamping force does not hinder orbarely hinders the detachment. In the fifth aspect, the prosthesis maybe one from the group of:

-   -   a ring prosthesis according to the second aspect of this        application; and/or    -   a stent according to the third aspect of this application;        and/or    -   a ‘prosthesis of the type with a tubular element’.        Sixth Aspect

According to a sixth aspect, this application relates to a new andinventive, variable-diameter ring structure with distal and proximalflange feet.

The object of the sixth aspect of this application is to provide a ringstructure of this type which is very simple in structure.

This object is achieved according to the sixth aspect by providing avariable-diameter ring structure with distal and proximal flange feet;wherein the ring structure has an axial direction and a radial directionacross it; wherein the distal and proximal flange feet have a radialposition, in which the free ends of the flange feet point in the radialdirection for anchoring with surrounding tissue; wherein the distalflange feet have an extended position, in which the distal flange feetextend in the radial direction; and

wherein the distal flange feet, when they are in the extended position,are under a pre-tension, which, when released, bends the distal flangefeet from the extended position to the radial position; and wherein thering structure is constructed from a series of elongated closed loopslying next to one another which, in each case, at the midpoint of thelongitudinal sides thereof, are attached laterally to one another via ajunction to form this ring structure, in such a way that, on the onehand, the imaginary line through all junctions forms a closed ring anddivides each loop into an aforementioned distal flange foot and anaforementioned proximal flange foot and, on the other hand, the ringstructure is expandable and/or compressible.

The simplicity is obtained according to the sixth aspect by constructingthe ring structure from elongated loops which, arranged with the longdirection in the axial direction of the ring structure, are set upalongside one another in an annular series and are connected roughly atthe midpoint of the long sides to the respective adjacent elongatedloop. The diameter of the ring structure can be varied due to the widthsof the loops, said widths being disposed in the circumferentialdirection of the ring structure. According to the sixth aspect, thesimplicity is further obtained by also using the elongated loops asproximal and distal flange feet, one half of the longitudinal loopsforming the proximal flange feet and the other half the distal flangefeet. In the extended condition, the loops are pre-tensioned in order tobe inclined to bend in a radially outward direction. It is noted herethat the proximal flange feet can also point permanently in the radialdirection, wherein only the distal part of the loops, under pre-tension,will then be able to be in the extended condition.

With regard to the distal and/or proximal flange feet of the ringstructure according to the sixth aspect of this application being in theextended condition under pre-tension, it is noted that this pre-tension,as explained at the beginning of this application in relation to activebending, can be implemented, on the one hand, by means of memorymaterials with memory properties which make it possible to ‘freeze’ theflange feet in the extended condition and/or, on the other hand, byusing conventional resilient materials.

Comparing the compressed and expanded diameter of the ring structure,according to the sixth aspect, viewed in relation to the expandedcondition, diameter reductions of more than 50% are achievable, i.e. thecompressed diameter may be less than half of the expanded diameter.

According to a further design of the sixth aspect, the distal flangefeet are bendable from the radial position to the extended positionagainst a resilience which builds up the aforementioned pre-tension. Thesurgeon or assistant will then himself extend the flange feet shortlybefore the intervention and fix them temporarily in the extendedposition by means of a mechanical obstacle and/or, in the case of amemory material, a temperature treatment.

According to a further design of the sixth aspect, the proximal flangefeet also have an extended position wherein the proximal flange feetextend in the axial direction; and the proximal flange feet, when theyare in the extended position, are under a pre-tension, which, whenreleased, bends the proximal flange feet from the extended position tothe radial position. The entire ring structure can thus be brought intoan essentially flat cylindrical condition.

According to a further design of the sixth aspect, the proximal flangefeet are bendable from the radial position to the extended positionagainst a resilience which builds up the aforementioned pre-tension. Thesurgeon or assistant will then himself extend the flange feet shortlybefore the intervention and fix them temporarily in the extendedposition by means of a mechanical obstacle and/or, in the case of amemory material, a temperature treatment.

According to a further design of the sixth aspect, the ring structure ismade from a memory material. The memory material here may be a memorymetal, such as a nitinol alloy.

According to a further design of the sixth aspect, the ring structure isexpandable from a first condition to a second condition, and the ringstructure, when it is in the first condition, is under a pre-tension,which, when released, causes the ring structure to expand in thedirection of the second condition. The ring structure can thereforeautomatically expand in full or in part. The expansion can neverthelessstill be supported by means of an instrument according to the firstaspect of the application, or by means of a different instrument, suchas a balloon.

According to a further design of the sixth aspect, the ring structure isexpandable from a first condition to a second condition, and the ringstructure, when it is in the second condition, is under a pre-tension,which, when released, causes the ring structure to contract in thedirection of the first condition. The ring structure can thereforeautomatically contract in full or in part. The ring structure istherefore usable, inter alia, as a constriction ring to constrict adilated heart valve or to draw the tissue around a heart valve moretightly against the prosthesis in order to prevent leakage outsidearound the prosthesis.

According to a further design of the sixth aspect, one or more of thejunctions is provided with one or more radial bores. This bore can beused to attach a biological or artificial valve prosthesis, stent, orfurther prosthesis to the ring structure. This can be done, for example,by means of a suture or with the aid of different attachment elementsfixable in the bores. This attachment of a further prosthesis can takeplace prior to or after the implementation of the ring structure in thepatient. Thus, for example, a valved stent according to the third aspectof this application can be implemented in combination with the ringstructure.

According to a further design of the sixth aspect with bores injunctions, at least 3, such as 4 or 8, junctions lying in a distributedmanner over the circumference of the ring structure have one or moreaforementioned radial bores. Thus, all junctions may also have one ormore aforementioned radial bores.

According to a further design of the sixth aspect, either the distalflange feet, in the radial position, have a bulge facing towards theproximal flange feet; or the proximal flange feet, in the radialposition, have a bulge facing towards the distal flange feet. Adaptationto the anatomy of the mitral and tricuspid annulus is thus implementedand a better attachment to the mitral or tricuspid annulus is possible.Here, the bulges may be provided in the halves of the respective flangefeet adjacent to the junction.

According to a further design of the sixth aspect, the ring structurecomprises a single piece of material. The ring structure may bemanufactured, for example, by laser burning or etching from a singlepiece. This single piece may be a tubular or otherwise plate material,for example made of metal such as stainless steel or a nitinol alloy. Ifthe ring structure is combined with a valved or non-valved stent, it ispossible to produce the combination of stent and ring structure from asingle piece of material, along with the possibility of producing thesetwo components as separate components and then interconnecting them atany time in a different manner, such as by means of sutures, welds orotherwise. The plate material may be in a flat or curved condition priorto the formation of the ring structure and may be closed to a ringstructure following removal of material, but the plate material may alsohave a tubular configuration prior to the removal of material.

According to further designs of the sixth aspect, the ring structure maybe sterile and/or made from one or more medically acceptable materials.

According to a further design of the sixth aspect, one or more of theflange feet comprises one or more pins on the sides facing towards oneanother. A firmer anchoring in tissue can thus be implemented ifrequired.

According to a further design of the sixth aspect, the ring structure orone or more flanges thereof, or one or more flange feet thereof aretotally or partially coated in a sealing manner with tissue, such aspericardium, or materials, such as textile or plastics which can betolerated by the body, such as Dacron and Teflon, which prevent thepassage of blood or other fluids.

According to a further design of the sixth aspect, one or both flanges,or the flange feet of one or both flanges thereof, differ from oneanother in length and/or in width and/or in shape and/or in angle inrelation to the longitudinal axis, or manner of coating and/or filling.

According to a further design of the sixth aspect, the separate flanges,or parts thereof, or the separate flange feet of the separate flangeshave an unequal shape and/or length and/or width in relation to oneanother, and/or angle in relation to the longitudinal axis, and/orfillings.

According to a further design of the sixth aspect, the fillings of theseparate flanges, or the separate flange feet of the separate flanges,have an unequal shape and/or length and/or width in relation to oneanother, and/or angle in relation to the longitudinal axis, and/orconsistency and/or material properties.

According to a further design of the sixth aspect, the fillings of theseparate flange feet extend beyond the circumference of a flange foot,and/or in a lateral and/or radial direction therefrom.

According to a further design of the sixth aspect, the fillings of theseparate flange feet are interconnected in such a way that a continuityarises between all or a number of fillings of the flange feet of one orboth flanges.

According to the sixth aspect, the application also relates to anassembly comprising a ring structure according to the sixth aspect alongwith a heart valve, which may or may not be stented or inserted in astent, mounted therein. The heart valve may be a natural donor valve,which may or may not be stented or inserted in a stent, such as from ananimal or human. In particular, the heart valve may comprise abiological material which is chosen from the group of:

porcine valves; and/or

bovine valves; and/or

equine valves; and/or

human valves; and/or

kangaroo valves.

As explained above in relation to the third aspect, it is also the casein the sixth aspect, as in the other aspects of this application, thatnone of these biological valves has to be entirely biological, but, inaddition to biological material, may also comprise non-biologicalmaterial such as plastic or metal. Furthermore, these biological valvesmay or may not be a reconstructed valve. A reconstructed valve isgenerally understood to be a valve of biological material, from whichthe original anatomical link has been broken. A reconstructed valve maybe formed by combining a plurality of biological components into avalve. The plurality of biological components may originate from thesame donor or from different donors. It is even conceivable for thebiological components to originate from different types of donor, forexample one or more components originating from a pig in combinationwith one or more components originating from a bovine animal, or one ormore components originating from a human in combination with one or morecomponents originating from the same or different types of animal.Seventh Aspect

According to a seventh aspect, this application also relates to amanipulator for releasing a prosthesis with a plurality of distal andproximal flange feet. Particularly in the case of compressibleprostheses, this cannot always be carried out in practice, in particularif the compressed prosthesis first needs to expand and only thereaftermust the flange feet be released from a radially pre-tensioned extendedposition to move to the radial position.

According to the seventh aspect, the object of this application is toprovide an alternative manipulator for the release of extended, radiallypre-tensioned distal and proximal flange feet.

This object is achieved according to the seventh aspect by providing amanipulator for the release of a prosthesis, wherein the prosthesis hasa plurality of distal and proximal flange feet, which:

-   -   have a radial position, in which the free ends of the flange        feet point in the radial direction for anchoring with        surrounding tissue;    -   have an extended position, in which the flange feet extend in        the radial direction; and,    -   if they are in the extended position, are under a pre-tension,        which, when released, bends the distal flange feet from the        extended position to the radial position;        wherein the manipulator comprises:    -   a plurality of U-shaped obstacle elements with a first leg and a        second leg, the free ends of which point in the distal        direction;    -   an operating element;    -   for each obstacle element, a cord, one end of which is attached        to the obstacle element and the other end of which is connected        to the operating element in such a way that, when the operating        element is displaced in the proximal direction, the obstacle        elements are retracted in the proximal direction.        With a manipulator of this type, the obstacle elements are each        connected separately via a cord to the operating element. The        operating element may be designed here in many different ways,        for example as a rod, tube, cord or any other element to which        cords are attachable. The U-shaped configuration of the obstacle        elements makes it possible to slide any obstacle from one edge,        the proximal edge, over the extended distal and proximal flange        feet and to hold it extended. The obstacle elements can then be        removed at a suitable moment when the prosthesis is at the        intervention site by retracting them in the proximal direction        by means of the cords and the operating element. The prosthesis        can be held in its position during this retraction by means of        an instrument or carrier to which the prosthesis is attached. It        is also possible for the prosthesis to be held in its position        during the retraction of the obstacle elements by the tissue        between which or to which the prosthesis must be attached. The        flange feet can bend to their radial position after the obstacle        organs have been removed therefrom. It may be possible here for        the obstacle elements, until the retraction thereof, to be held        in their position on the flange feet due to the proximal flange        feet being inclined, as a result of their pre-tension, to bend        within the opening defined between the legs of the U-shape. The        proximal flange feet will brace themselves between the legs and        will be inclined to hold them in place.        The manipulator according to the second aspect may be used        entirely separately from other instruments or tools for        implanting a prosthesis. However, the manipulator according to        the seventh aspect is also very readily applicable in        combination with an instrument/applicator according to the first        aspect, in combination with an applicator or other tool for        implanting the prosthesis as known from one of the earlier        applications of the inventor (the aforementioned WO 00/24339, WO        00/44311, WO 03/003926, WO 03/082121 and WO 2005/092246), such        as a sleeve which holds the prosthesis in the compressed        condition, or otherwise. If a tool, such as a sleeve (which is        also understood to include a tube), holds the prosthesis in the        compressed condition, this offers the advantage, in cases where        the manipulator according to the seventh aspect is used, that        the tool can first be removed to allow the prosthesis to expand        and that, for example after the expansion has taken place, the        U-shaped obstacle elements are removable in the second instance        independently from the tool by retracting them in the proximal        direction.

According to a further embodiment of the seventh aspect, in the extendedcondition of the flange feet, a first length is defined in themanipulator as the axial distance between the free ends of distal andproximal flange feet; the first legs of the obstacle elements have asecond length; and the second length is at least 75%, such as 90%, ofthe first length. The first legs can thus extend sufficiently far fromthe radial outside of the prosthesis along the flange feet to hold boththe proximal and the distal flange feet in the extended condition. Ifthe second length here is greater than the first length, the first legscan entirely cover the proximal and distal flange feet from outside andeven extend beyond them. The risk of the flange feet then damagingsurrounding tissue can therefore be reduced.

According to a further design of the seventh aspect, the second legs areshorter than the first legs. The second legs lie on the radial inside ofthe prosthesis. In the extended condition, the flange feet arepre-tensioned in order to be inclined to bend radially outwards. They donot then need to be held in place from the inside. The function of thesecond leg is primarily to hold the obstacle element on the proximalflange foot, for example in that the proximal flange foot, as alreadyexplained above, braces itself between the legs of the U-shapedobstacle.

According to a further design of the seventh aspect, the proximal flangefeet have a third length, wherein the second legs have a fourth length;and wherein the fourth length is at most equal to the third length. Thesecond legs, which will lie on the inside of the prosthesis, will nottherefore extend beyond the proximal flange feet. Damage from partsprovided within the prosthesis, such as donor tissue, valve flaps orother construction parts, is thus avoided. If the fourth length is atleast 75% of the third length, bracing of the proximal flange feetbetween the legs can be very reliably ensured.

According to the seventh aspect, the application also relates to anassembly comprising a manipulator according to the seventh aspect and aprosthesis, wherein the prosthesis has a plurality of distal andproximal flange feet, which:

-   -   have a radial position, in which the free ends of the flange        feet point in the radial direction for anchoring with        surrounding tissue;    -   have an extended position, in which the flange feet extend in        the axial direction; and,    -   if they are in the extended position, are under a pre-tension,        which, when released, bends the distal flange feet from the        extended position to the radial position.

According to a further design of the assembly according to the seventhaspect, a heart valve, which may or may not be stented or inserted in astent, can be mounted in the prosthesis. The heart valve may be anatural donor valve, which may or may not be stented or inserted in astent, such as from an animal or human. In particular, the heart valvemay comprise a biological material which is chosen from the group of:

-   -   porcine valves; and/or    -   bovine valves; and/or    -   equine valves; and/or    -   human valves; and/or    -   kangaroo valves.        As explained above in relation to the third and sixth aspect, it        is also the case in the seventh aspect, as in the other aspects        of this application, that none of these biological valves has to        be entirely biological, but, in addition to biological material,        may also comprise non-biological material such as plastic or        metal. Furthermore, these biological valves may or may not be a        reconstructed valve. A reconstructed valve is generally        understood to be a valve of biological material, from which the        original anatomical link has been broken. A reconstructed valve        may be formed by combining a plurality of biological components        into a valve. The plurality of biological components may        originate from the same donor or from different donors. It is        even conceivable for the biological components to originate from        different types of donor, for example one or more components        originating from a pig in combination with one or more        components originating from a bovine animal, or one or more        components originating from a human in combination with one or        more components originating from the same or different types of        animal.

According to a further design of the assembly according to the seventhaspect, the prosthesis is one from the group of:

-   -   a ring prosthesis according to the second aspect; and/or    -   a stent according to the third aspect; and/or    -   a ring structure according to the sixth aspect; and/or    -   a stented valve prosthesis; and/or    -   a ‘prosthesis of the type with a tubular element’.

According to a further design of the assembly according to the seventhaspect, the assembly further comprises a sleeve (which is alsounderstood to mean a tube) with a diameter smaller than the maximum orexpanded diameter of the prosthesis.

Eighth Aspect

According to an eighth aspect, this application also relates to a portassembly. A port is a construction which provides a passage through awall into the body or an organ of the patient. Ports of this type may beof a temporary or permanent or semi-permanent nature. In the case of apermanent or semi-permanent port, the connector provided on the outsideof the passage for connection of tools is left behind in or on thepatient. The difference between a semi-permanent and a permanent port isessentially that the semi-permanent port does not remain indefinitely inor on the patient.

In the case of a connector for a permanent or semi-permanent port, it isimportant that a) the connection on the wall with the passage formed orpassage still to be formed therein can be easily made and maintained,and b) this connection also forms a reliable seal. A first object of theeighth aspect of this application is to provide a port assembly whichmeets this requirement.

This first object is achieved according to the eighth aspect byproviding a port assembly, comprising:

-   -   an annular connector which surrounds a port passage; and    -   a sealing cap to seal the port passage;        wherein the port passage extends from a first connector end to a        second connector end;        wherein the second connector end comprises a crosswise contact        surface to lie against a wall of an organ;        wherein, in the crosswise contact surface, at least one adhesive        slot, such as two adhesive slots, is provided, which extends        around the port passage and which is connectable via a feed        channel which opens out into this slot to a source for tissue        adhesive; and        wherein, in the crosswise contact surface, at least one ring,        such as two rings, of one or more suction mouths is provided,        said ring extending around the port passage and being        connectable via a suction channel to a suction source to suck        the crosswise contact surface firmly against the wall of the        organ.

The connector will lie here from the access side against the outer wallof the organ (or the body) of the patient. The at least one ring ofsuction mouths enables a very reliable and very quickly implementableattachment to the wall of the organ concerned. The suction force exertedvia a suction source on the suction mouths sucks the connector firmlyagainst the wall of the organ. The at least one adhesive slot whichextends around the port passage enables, on the one hand, a veryreliable sealing and, on the other hand, enables a permanent orsemi-permanent attachment of the connector to the wall of the organconcerned. Tissue adhesive can be brought from the adhesive source intothe adhesive slot, with which the connector can be firmly adhered to thewall of the organ. Due to the fact that the adhesive slot extends aroundthe passage, sealing can be ensured around the entire passage. If theport is not or is no longer used to provide access into the organconcerned, the port can be sealed by means of the sealing cap. Thesealing cap can provide a permanent seal and then no longer needs to beremovable. However, the sealing cap will, in particular, be removableonce more to provide further access into the organ. For this purpose,the connector and sealing cap can be provided with a first matinginterlocking mechanism, such as a bayonet connection or screw thread,with which the connector and sealing cap are attachable to one anotherin a manner which seals the port passage.

According to a further design of the eighth aspect, the first matinginterlocking mechanism comprises an inner screw thread provided on theconnector and an outer screw thread provided on the sealing cap. Thus,when the port is closed, the port passage located within the connectorcan also be filled. Thus, when the port is closed, fluid, such as blood,can be prevented from occurring or accumulating therein. It isparticularly expedient here if the inner screw thread extends to thecrosswise contact surface. Depending on the thickness of the wall of theorgan to which the port is attached, it can be expedient here if thesealing cap can be rotated beyond the crosswise contact surface in theconnector so that it also fills the passage in the wall of the organ.The purpose of this is to prevent the accumulation of body fluids inthis passage. Alternatively, the opening in the body tissue can also besealed directly and in a manner other than by means of the cap describedhere. In this case, the remainder of the eighth aspect can be usedwithout a cap, and the connector can be attached only temporarily to ahollow organ, and can also be removed again from the body without beingfinally attached to the hollow organ. In such a case, the eighth aspectwill be able to be temporarily attached to a hollow organ by sucking theconnector firmly to the organ and the use of adhesive can be dispensedwith.

According to a further design of the eighth aspect, the at least onering of suction mouths comprises at least one suction slot, such as twosuction slots, which extend around the port passage. A firm suction canthus be ensured completely around the port passage.

According to a further design of the eighth aspect, the port assemblyfurther comprises an adhesive source for tissue adhesive and/or asuction source to generate a suction force in the at least one ring ofone or more suction mouths.

According to a further design of the eighth aspect, the port assemblyfurther comprises one or more work channels which are connectable in adisconnectable manner to the first connector end. A work channelsimplifies the remote implanting of the connector, the remote insertionof instruments and the remote fitting of the cap. The remote workingfacility allows the operator to work via small incisions and to carryout the entire intervention in a minimally invasive manner. A workchannel also makes it possible to create a defined required climate inthe port, for example by gassing and/or ventilation and/or irrigationand/or drainage. A climate of this type can serve to protect the patientand/or can serve to prevent body fluids from flowing away excessivelyduring an intervention.

According to a further design of the eighth aspect, the work channelcomprises a stiff or stiffened channel part and a flexible channel partwhich is provided between the connector and the stiff channel part insuch a way that the stiff channel part is pivotable in relation to theconnector. Stiffness of the work channel is important to enable aninstrument to be easily guided through it. The instrument may otherwisebe caught up or obstructed as a result of flexibility of the workchannel. On the other hand, a stiff work channel following on from theconnector is not very practical because this imposes restrictions on theaccessibility of the connector for the work channel and because theconnector may then come loose during manipulation of the work channel.This is solved by providing a flexible channel part between the stiffpart of the work channel and the connector. In particular, this flexiblechannel part follows on directly from the connector.

In the case of a port, it is important for the work channel to be stiff,for example because an instrument guided through the work channel mayotherwise be hindered by the work channel in the movement of theinstrument, or because the connector cannot otherwise be remotelynavigated and implanted. However, a stiff work channel following on froma connector has the disadvantage that the connector restricts the angleat which work can be carried out by the operator and may inadvertentlycome loose during manipulation of the work channel. A second object ofthe eighth aspect of this application is to provide a port assemblywhich overcomes this problem.

According to a further design of the eighth aspect with a flexible workchannel part, the flexible work channel part will be able to have alength of at most 20%, such as at most 10%, of the length of the stiffor stiffened channel part.

According to a further design of the eighth aspect with a flexible workchannel part, the length of the flexible channel part may be up to 3times, such as at most 2 times, the diameter of the port passage,whereas the length of the stiff or stiffened channel part may be morethan 10× the diameter of the port passage, such as 20× or more than 30×the diameter of the port passage.

This second object of the eighth aspect is achieved by providing a portassembly, comprising:

-   -   an annular connector which surrounds a port passage, said port        passage extending from a first connector end to a second        connector end; and    -   one or more work channels which are connectable in a        disconnectable manner to the first connector end;        wherein the second connector end comprises a crosswise contact        surface for placing against a wall of an organ; and wherein at        least one of these work channels, such as all of these work        channels, comprises a stiff or stiffened channel part and a        flexible channel part which is provided between the connector        and the stiff channel part in such a way that the stiff channel        part is pivotable in relation to the connector.

According to a further design of the eighth aspect with a flexible workchannel part, the flexible work channel part will be able to have alength of at most 20%, such as at most 10%, of the length of the stiffor stiffened channel part.

According to a further design of the eighth aspect with a flexible workchannel part, the length of the flexible channel part may be up to 3times, such as at most 2 times, the diameter of the port passage,whereas the length of the stiff or stiffened channel part may be morethan 10× the diameter of the port passage, such as 20× or more than 30×the diameter of the port passage.

According to a further design of the eighth aspect:

-   -   the assembly further comprises a sealing cap to seal the port        passage; and/or    -   the connector and the work channel are provided with a second        mating interlocking mechanism, such as a bayonet connection or a        screw thread, with which the connector and the work channel are        attachable to one another in a sealing manner; and the second        mating interlocking mechanism here may comprise an outer screw        thread provided on the connector and an inner screw thread        provided on the sealing cap.

According to a further design of the eighth aspect, the end of the workchannel facing away from the connector is provided with a seal which isdesigned, on the one hand, to seal the access to the passage surroundedby the work channel and, on the other hand, to allow through aninstrument which is to be inserted inwards into the work channel, whilemaintaining the seal. A seal of this type may, for example, comprise avascular prosthesis or comparable element. A vascular prosthesis cansimply be squeezed tight with the hand, a clamp or wire, elastic orotherwise.

According to a further design of the eighth aspect, the work channel isprovided with at least one connection, such as two, three or fourconnections, for gassing and/or degassing and/or irrigation and/ordrainage of the passage surrounded by the work channel; and/or the workchannel is provided with one or more valves in order to counteract bloodloss on the one hand and, on the other hand, to prevent air fromentering.

According to a further design of the eighth aspect, the connector isproduced from soluble, so-called ‘bioabsorbable’ or ‘biodegradable’materials, so that the connector can wholly or partially dissolvethrough time.

According to a further design of the eighth aspect, the cap is coated onthe crosswise side with antithrombotic materials or chemical componentsto prevent blood clotting in situ, or is covered with a piece ofvascular prosthesis, or human or animal pericardium, or other materialto promote the growth of endothelial tissue in situ.

According to a further design of the eighth aspect, the connector isprovided with one or more contact and/or pressure sensors on thecrosswise edge to determine whether there is sufficient tissue contactbetween the crosswise edge of the connector and the tissue where this islocated.

Ninth Aspect

According to a ninth aspect, this application relates to a method forimplanting a valve prosthesis in a passage through which blood flows,and also a valve prosthesis which is particularly suitable for thispurpose. This method and this assembly are involved in several places inthis application in relation to embodiments of aspects discussedtherein. The method according to the ninth aspect comprises thefollowing steps:

-   -   the insertion into the passage and attachment to surrounding        tissue of a ring prosthesis which, under pre-tension, is held in        a first diameter, wherein the pre-tension tends to constrict the        ring prosthesis to a smaller, second diameter;    -   the insertion into the passage of the valve prosthesis;    -   the release of the pre-tensioned ring prosthesis in such a way        that, under the influence of the pre-tension, it draws the        tissue surrounding the passage against the valve prosthesis.        The valve prosthesis is in particular a heart valve prosthesis,        and comprises:    -   at least a first radial flange provided with radial slots;    -   pins which project through the slots in a radial direction;    -   a tensioning mechanism designed to be able to pre-tension the        pins in order to move through the slots in a radially inward        direction; and    -   a heart valve.        Further designs of the ninth aspect of the application are set        out in the claususes 192-207 associated with the ninth aspect,        and also at various places in relation to other aspects of this        application. As far as the method and valve prosthesis according        to the ninth aspect are concerned, these explanations of the        ninth aspect in the other aspects of this application must be        interpreted more broadly than as if only restricted to the        design of the relevant other aspect discussed therein.

It is noted that each aspect in this application is one invention orcomprises a plurality of inventions.

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention will be explained below with reference toembodiments shown schematically in the drawings. In the drawings:

FIGS. 1A and 1B show a schematic, perspective view of a medicalinstrument, in a use as an applicator, according to the first aspect;wherein FIG. 1A shows a condition in which the manipulator holds theprosthesis in place, and FIG. 1B shows a condition in which themanipulator has released the prosthesis;

FIGS. 2A and 2B show schematic longitudinal perspectives of the medicalinstrument according to FIGS. 1A and 1B, wherein FIG. 2A shows acondition in which the manipulator holds the prosthesis in place andFIG. 2B shows a condition in which the manipulator has released theprosthesis;

FIGS. 3A and 3B show a schematic, longitudinal section view of a secondembodiment of a medical instrument, used as an applicator, according tothe first aspect; wherein FIG. 3A shows a condition in which themanipulator holds the prosthesis in place and FIG. 3B shows a conditionin which the manipulator has released the prosthesis;

FIG. 4 shows a schematic, longitudinal section view of a thirdembodiment of a medical instrument, used as an applicator, according tothe first aspect;

FIGS. 5A-5C show a schematic, longitudinal section view of a fourthembodiment of a medical instrument according to the first aspect, inthis case used as an applicator for a stent, which may also be a valvedstent; wherein FIG. 5A shows a condition in which the manipulator holdsa compressed stent in place; FIG. 5B shows a condition in which themanipulator holds an expanded stent in place, and FIG. 5C shows acondition in which the manipulator has released the expanded stent;

FIGS. 6A-6D show a schematic, longitudinal section view of a fifthembodiment of a medical instrument according to the first aspect, inthis case used as an applicator for a stent, which may also be a valvedstent; wherein FIG. 6A shows a condition in which the manipulator holdsthe compressed prosthesis in place; FIG. 6B shows a condition in whichthe manipulator holds the expanded prosthesis in place; FIG. 6C shows acondition in which the manipulator partially releases the expandedprosthesis in place; FIG. 6D shows a slightly later condition in whichthe manipulator has partially released the expanded stent;

FIGS. 7A-7C show a schematic, longitudinal section view of a sixthembodiment of a medical instrument according to the first aspect, inthis case used as an applicator for a stent, which may also be a valvedstent; wherein FIG. 7A shows a condition in which the manipulator holdsthe compressed stent in place; FIG. 7B shows a condition in which themanipulator holds the expanded stent in place; FIG. 7C shows a conditionin which the manipulator has released the expanded stent;

FIGS. 8A-8C show a schematic longitudinal section view of a seventhembodiment of a medical instrument according to the first aspect,wherein the medical instrument is used as an applicator for a ringprosthesis according to the second aspect; wherein FIG. 8A shows acondition in which the manipulator carries the ring prosthesis, FIG. 8Bshows a condition in which the manipulator has detached the ringprosthesis, and FIG. 8C shows a condition in which the manipulator isretracted from the ring prosthesis;

FIGS. 9A and 9B show a schematic view of a first design of a ringprosthesis according to the second aspect, as also shown in FIGS. 8A-8C;wherein FIG. 9A is a perspective view and FIG. 9B is a side view;

FIGS. 10A and 10B show a schematic longitudinal section view of aneighth embodiment of a medical instrument according to the first aspect,wherein the medical instrument is used as an applicator for a ringprosthesis according to the second aspect; wherein FIG. 10A shows acondition in which the manipulator carries the ring prosthesis while thelatter has a large diameter, and FIG. 8B shows a condition in which themanipulator carries the ring prosthesis while the latter has a smallerdiameter;

FIGS. 11A and 11B show a schematic view of a second design of a ringprosthesis according to the second aspect, as also shown in FIGS. 10Aand 10B; wherein FIG. 11A is a perspective view and FIG. 11B is a sideview;

FIGS. 12A and 12B show, in perspective side view, a third design of aring prosthesis according to the second aspect; wherein FIG. 12A shows aview obliquely from above and FIGS. 12A and 12B show a view of the sideedge of the ring (with the so-called clamping mouths in FIG. 12Bsubstantially schematised);

FIGS. 13A and 13B show a very simply designed applicator according to afifth aspect with a ring prosthesis according to the second aspectloaded thereon; here, FIG. 13A shows a perspective view and FIG. 13Bshows a longitudinal section view of the distal part of this applicator;

FIGS. 14A and 14B show a schematic longitudinal section of a ninthdesign of a medical instrument according to the first aspect; whereinFIG. 14A shows a condition with the fingers at the minimum span, andFIG. 14B shows a condition with the fingers at the maximum span;

FIG. 15 shows a schematic longitudinal section of a first design of aprosthesis according to the fourth aspect of this application; whereinFIG. 15 is a modified version of FIG. 10A from WO 00/24339 of theinventor;

FIGS. 16A and 16B show a schematic longitudinal section of a seconddesign of a prosthesis according to the fourth aspect of thisapplication; wherein FIG. 16A shows the condition with extended proximaland distal flange feet, and FIG. 16B shows the condition wherein theproximal and distal flange feet are in the radial position; and whereinFIGS. 16A and 16B are a modified version of FIGS. 2A and 2B from WO00/44311 of the inventor;

FIG. 17 shows an opened, flatly laid out view of a ring structureaccording to the sixth aspect;

FIG. 18 shows a schematic side view in cross-section of the ringstructure shown in FIG. 17 , wherein the ring structure is shown in boththe contracted position and in the expanded position;

FIG. 19 shows a schematic cross-section view of the heart, with anassembly of a ring structure and a valve stent implanted therein in themitral valve position;

FIG. 20 shows a very schematic representation of a manipulator accordingto the eighth aspect for the release of a prosthesis;

FIGS. 21A and 21B show details of the obstacle element of themanipulator according to FIG. 20 , wherein FIG. 21A shows the obstacleelement in the condition in which a proximal and distal flange foot areheld extended, and FIG. 21B shows the condition in which these flangefeet have been released;

FIG. 22 shows a perspective view of a longitudinal section of a portassembly according to the eighth aspect;

FIG. 23 shows a very schematic longitudinal section of a further portassembly according to the eighth aspect; and

FIGS. 24A and 24B show, very schematically, an assembly and methodaccording to the ninth aspect, wherein FIG. 24A shows a top view andFIG. 24B shows a detail.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

FIGS. 1A, 1B, 2A and 2B show a first embodiment 100 of a medicalinstrument according to the first aspect. The medical instrument is usedhere as an applicator 100 for implanting a prosthesis, in particular aheart prosthesis. This prosthesis is of a type as described in earlierPCT applications of the inventor, i.e. WO 00/24339, WO 00/44311, WO03/003926, WO 03/082121 and WO 2005/092246.

The applicator 100 comprises a first rod 1 in the form of a tube, asecond rod 2, as shown in FIGS. 2A and 2B, which extends along andparallel to the tube 1, in this case the second rod 2 being pushedthrough the tube 1, a longitudinal centre line 3 and also a manipulator140. The longitudinal centre line 3 is defined here by the direction inwhich the tube 1 and the second rod 2 extend. The second rod 2 can beshifted in relation to the tube 1 by shifting the rod 2 in the extensiondirection of the longitudinal centre line 3 in relation to the tube 1.In order to limit this longitudinal shift, the tube 1 is provided withlongitudinal slots 21, and a pin 22 which projects into the longitudinalslot 21 is provided on the second rod. In order to be able to move thesecond rod 2 in relation to the tube 1, an operating button 25 isprovided on the proximal end of the applicator. As shown in particularin FIG. 2A, this operating button 25 is provided with an inner screwthread 24 which interworks with an outer screw thread 23 provided on theproximal end of the tube 1. On the proximal end of the second rod 2, acarrier 26 is provided which is widened in relation to the second rodand is confined in the operating button 25 in such a way that theoperating button 25 is freely rotatable in relation to the carrier 26,which in turn is again fixed in relation to the second rod 2. Throughrotation of the operating button 25, depending on the direction ofrotation, the second rod 2 is displaced in relation to the tube 1 in thedistal direction D or proximal direction P. As the pin 22 in thelongitudinal slot 21 prevents rotation of the second rod 2 in relationto the tube 1, the movement of the tube 1 in relation to the second rod2 will be a pure translation movement here.

In order to enable the operator to handle the medical instrument in asimple manner, the instrument is provided with a handgrip 27 (not shownin FIG. 1B).

It will be clear that the part 14 of the applicator (see FIG. 1B) may belonger or shorter, as required for the application. Furthermore, it isnoted that the applicator, viewed in relation to the longitudinal centreline 3, does not have to be rigid. Discussed in terms of thelongitudinal centre line 3, the applicator may be designed to bebendable and/or kinkable and/or flexible, so that it is also usable ifthe access route to the intended location for the distal end 15 of theapplicator runs along a non-straight route. In particular, theaforementioned part 14 of the applicator will be able to be designed tobe bendable and/or kinkable and/or flexible for this purpose. It willfurthermore be clear that the comments made in this paragraph areapplicable to all designs of the first aspect of this application. Theflexible and/or bendable and/or kinkable characteristic of theapplicator can be implemented by designing the aforementioned part 14,i.e. the rods running there, in nitinol in superelastic form or inwires, such as steel wires.

The applicator shown in FIGS. 1A, 1B, 2A and 2B is furthermore providedon the distal end with a ‘prosthesis 40 of the type with a tubularelement’. This prosthesis 40 comprises a proximal flange 41, a tubularelement 42 and a distal flange 43. The distal flange 43 is constructedfrom flange feet 44 which move from the axial, extended position shownin FIGS. 1A, 1B and 2A to the radial position indicated in FIG. 2B bybroken lines (on the right-hand side). Thus, the proximal and distalflange can clamp tissue, such as the annulus tissue of a heart valve, inorder to fix themselves in a bloodstream passage. This is known per sefrom the previously repeatedly mentioned earlier PCT applications of theinventor. In the embodiment shown in FIGS. 1A, 1B, 2A and 2B, theproximal flange 41 is a fixed flange which extends continuously in theradial direction from the tubular element 42. In this case, the proximalflange 41 is furthermore designed as interrupted with interruptions 45located at—in this case regular—intermediate intervals. However, it isnoted that the proximal flange 41 may also be designed as uninterruptedand/or movable, in the same way as the distal flange 43.

The applicator 100 is provided with a carrier part 28 to carry theprosthesis 40. As an intermediate piece between the carrier part 28 andthe prosthesis 40, a waved ring 29 is provided, with four wave peaks 31and four wave troughs 30 (as shown in particular in FIGS. 1A and 1B).This waved ring carries the prosthesis 40 with the wave troughs, so thatthe prosthesis 40 is essentially carried at four points. This simplifiesthe detachment of the prosthesis after it has been attached tosurrounding tissue. If the prosthesis 40 serves to attach a newartificial heart valve or donor heart valve, it is possible in principleto choose to attach the new artificial heart valve or donor heart valvein advance in the ring prosthesis. The heart valve is then loaded ontothe applicator together with the prosthesis 40. Following detachment andattachment to tissue of the prosthesis 40, no further assembly actionneeds to be carried out for the attachment of a heart valve. However, itis also very readily possible first to attach the prosthesis 40 tosurrounding tissue and only thereafter to implant the new artificialheart valve or donor heart valve and attach it to the prosthesis 40. Ifthe prosthesis 40 is first attached to the tissue and the valve isimplanted thereafter, it is conceivable that the applicator 100 is firstremoved from the patient and that the same or a different applicatorprovided with the valve is thereafter delivered to the interventionlocation in order to implant the valve. It is also conceivable first toimplant the prosthesis 40 with a single applicator and then, withoutfirst retracting the applicator from the patient, to insert the valveinto the already implanted prosthesis.

The manipulator 140 of the applicator 100 comprises a first plurality offingers 4, each with a first finger end 5 and a second finger end 6. Thesecond finger end 6 is a free end and the first finger ends 5 aresupported on the second rod 2. In the case of FIGS. 1A, 1B, 2A and 2B,the support of the first finger ends 5 takes place on the second rod 2via a pivot attachment in such a way that the fingers 4 are pivotable inrelation to the rod 2. In this case, the pivot attachment is designed asa hinge with a convex hinge part 32 attached to the second rod 2 and aconcave hinge part 33 provided at the first finger end 5 to accommodatethe convex hinge part 32. It is noted that the pivotable attachment mayalso be designed in a different manner, for example by means of a forkhinge, i.e. a forked part, of which the fork forms the pivot centreline, is formed on the first finger ends, but the pivot attachment mayalso be designed in a different manner known per se to the personskilled in the art; or by means of a ring which is pushed throughpassages in the fingers, wherein the fingers are, as it were, threadedonto the ring and the ring acts as a hinge axis for the fingers.

In the condition shown in FIGS. 1A and 2B, the free finger ends 6overlap the distal flange feet 44 extended in the axial direction. Theterm ‘overlap’ is understood in this application to mean that, viewed inthe radial direction perpendicular to the longitudinal centre line 3 ofthe medical instrument, there is an overlap between the free finger ends6 of the relevant fingers and the prosthesis, in this case the flangefeet 44 thereof. In this overlapping condition, the fingers 4 preventthe distal flange feet 44 from being able to move from the axiallyextended position to the radial position, indicated schematically inFIG. 2B with a broken line. As will be clear, it is practical here ifthe fingers 4 in the overlapping position are prevented from pivotingradially outwards. This can be implemented as such in many differentways. Thus, for example, a spring or other tensioning element can bedisposed around the fingers 4. However, it is also very readily possibleto confine the fingers 4 by means of a guide in the position shown inFIG. 2A, as will be further explained below.

The condition shown in FIG. 1A and FIG. 2A is also the condition inwhich the prosthesis is delivered by means of the applicator to itsintended position in the organ or otherwise in the patient, referred toas the intervention location. During this delivery to the interventionlocation, the fingers in the overlapping position then ensure that thedistal flange feet remain in the axially extended condition. During thisdelivery of the prosthesis to the intervention location, the applicatorwill be fed in the distal direction through a channel of tissue, such asa blood vessel. The free second finger ends 6 will protect the distalflange feet 44, which are overlapped by these free second finger ends 6,from the channel wall and hold them in the extended axial position.

After the prosthesis has arrived at its intended location and has beencorrectly positioned there, the tube 1 will be held immovably inrelation to the intended location and the second rod 2 will be displacedin the distal direction D in relation to the tube 1 through operation ofthe rotary button 25. The fingers 4 attached via a pivot attachment tothe second rod 2 will be displaced in the distal direction D in relationto the prosthesis 40. The free second finger ends 6 come free from theaxially extended distal flange feet 44. The distal flange feet 44 canthen bend actively or passively to the radial position. With referenceto FIG. 2A, it is clear that, if the fingers 4 are shifted in the distaldirection D in relation to the tube 1, the fingers are then initiallyshifted purely distally as long as the fingers 4 are supported on theflat part of the guide 51 which runs parallel to the longitudinal centreline 3. As soon as the fingers 4 arrive with their curved part 9 at theoblique part 12 of the guide, a combined movement will take place,comprising a translation of the fingers in the distal direction and arotation around the pivot point 32.

As is evident, in particular in FIG. 2B, the free second finger ends 6pivot, during the displacement in the distal direction of the rod 2, inthe radially inward direction towards the longitudinal centre line 3 ofthe applicator 100. The free ends 6 of the fingers 4 therefore move herefrom a first position (shown in FIGS. 1A and 2A) to a second position(shown in FIGS. 1B and 2B), wherein the distance from the free ends 6 ofthe fingers 4 to the longitudinal centre line 3 is shorter than in thefirst position. In the second position, also referred to as the releaseposition, the fingers 4 therefore lie closer against the longitudinalcentre line 3. The span X of the applicator 100 is therefore reduced, atleast at the location of the fingers 4. The term ‘span’ is understoodhere to mean the space that the medical instrument occupies at thelocation of the fingers in a direction across the longitudinal centreline 3. In the embodiment shown in FIGS. 2A and 2B, the span X in therelease position according to FIG. 2B is around 62% of the span X inFIG. 2A in the overlapping position. Thus, the distal part of theapplicator 100 indicated as Y in FIG. 2B, i.e. the part which is locateddistally in relation to the prosthesis, can easily pass, in the releaseposition, in the proximal direction P through the inside of theprosthesis 40, to remove the tube 1, the second rod 2 and themanipulator 140 from the patient, leaving behind the prosthesis.

As clearly shown in FIGS. 1A, 1B, 2A and 2B, the applicator 100,according to a further design, is provided distally from the carrierpart 28 with a slotted element 34, which, in the embodiment shown, isdesigned as a unit integrated with the carrier part 28. However, it willbe clear that the slotted element can also be a component providedseparately on the tube 1. Each finger 4 extends through a slot 35 of theslotted element 34. In the overlapping position, shown in FIGS. 1A and2B, the fingers 4 project from the slots 35. In the release position,shown in FIGS. 1B and 2B, the fingers 4 are entirely sunk into the slots35 in order to be protected from the environment by the slotted element34. When the applicator is retracted after the prosthesis has beendelivered, the fingers 4 cannot therefore damage any tissue, includingany heart valve tissue, along which they pass. The fingers are at anyrate protected from that tissue by the slotted element 34.

As shown particularly in FIGS. 2A and 2B, the slots 35 have slot bases36. The slot bases 36 extend along a curve to the carrier part 28,viewed from the distal end to the proximal end of the instrument, to endbeyond the lower ends of the distal flange feet 44. It is thereforepossible, after the distal flange feet 44 have been released by thefingers 4, to further use the fingers to press therewith from the insideout against the distal flange feet 44 in order to bend them to theirradial position. The same can furthermore also be achieved by deepeningthe slot bases 36 so that, in the overlapping position, a slit (at 49 inFIG. 2A) is located between the slot base 36 and the respective fingers4. These slits ensure that the fingers 4, as soon as they come free,from the overlapping position, from the distal flange feet 44, as itwere, spring inwards in the radial direction. If the fingers are thenmoved once more in the proximal direction in relation to the tube 1,they will be able to press against the inside of the distal flange feet44 to help the latter in the pivoting thereof in the radial direction.If the distal flange feet 44 cannot bend automatically, for exampleunder the influence of a pre-tension, from an axial to a radialposition, it may be possible that the fingers 4 entirely ensure thisbending of the flange feet from the axial to the radial position. Thefingers 4 can therefore bend the distal flange feet actively to theradial position without a passive or otherwise prior bending beingrequired.

According to a further embodiment of the applicator shown in FIGS. 1A,1B, 2A and 2B, an annular outer guide 37 is optionally provided. Thisguide is located distally from the carrier part 28 and also distallyfrom the slotted element 34. The annular outer guide 37 is attached tothe tube 1 and is preferably fixed in relation to the tube 1. The axialcentre line of the annular outer guide 37 is, in particular, parallel tothe longitudinal centre line 3 and, in the embodiment shown, coincideswith the longitudinal centre line 3 of the medical instrument. As shownin FIGS. 2A and 2B, the fingers 4 project in the axial direction throughthe annular outer guide 37. The first finger ends 5 lie here distallyfrom the annular outer guide 37 and the free, second finger ends 6 liehere proximally from the annular outer guide 37. The distance from thefirst finger ends 5 to the longitudinal centre line 3 is less than theradius of the annular outer guide 37. The free, second finger ends 6lie, in the overlapping position, at a distance from the axial centreline of the annular guide 37 which is greater than the radius of theannular guide in order to lie, in the release position, at a distancefrom the axial centre line of the annular guide 37 which is smaller thanthe radius of the annular guide. The annular outer guide 37 guides thefingers, during the displacement of the rod from the overlappingposition to the release position, in a radially inward direction towardsthe longitudinal centre line 3 of the applicator.

In the embodiment shown, although this may also be different, theannular outer guide 37 is formed by the proximal edge of a sleeve 38.This sleeve protects fingers 4 retracted therein from the environment.

According to a further embodiment, a support ring 39, which is attachedby means of carrier arms 46 on an adjustment part 47, may optionally beprovided. The adjustment part 47 is adjustable along the tube 1 and isfixable, for example by means of a screw 48, to the tube 1 in a requiredposition. In the condition shown in FIGS. 1A, 1B, 2A and 2B, the supportring 39 lies at a distance from the prosthesis. The purpose of this isto maintain greater clarity in the illustrations shown in FIGS. 1A, 1B,2A and 2B. However, if the support ring 39 is used, it will normally liefrom the proximal side against the prosthesis 40. The support ringtherefore supports the prosthesis from the proximal side if a forceacting in the proximal direction is exerted on the prosthesis. This maybe the case, for example, if the prosthesis has to be pushed with forcethrough a constriction, or if the distal flange feet 44, in the radialposition, are pushed with force in the proximal direction. In order, onthe one hand, to provide a clearer view and, on the other hand, also toprovide space, for example, for stented parts of a biological tissue or,for example, for artificial or biological valve flaps, the support ring39 is designed to be open and is attached by means of carrier arms 46 tothe adjustment part 47.

According to a further embodiment, the medical instrument, in the caseof FIGS. 1A, 1B, 2A and 2B, comprises an applicator, optionally an innerguide 51 and an outer guide 52, both of said guides being carried by thefirst rod, in this case the tube 1. Here, the fingers 4 each have afirst curved zone 9. The fingers 4 define an inner longitudinal side 7here facing towards the longitudinal centre line 3 and an outerlongitudinal side 8 facing away from the longitudinal centre line 3. Theinner guide 51 is provided between the longitudinal centre line 3 andthe inner longitudinal side 7 of the fingers. The fingers 4 arefurthermore provided between the outer guide 52 and the longitudinalcentre line 3. The aforementioned first curved zone 9 of each fingerdefines a first finger part 10, which extends from the first finger end5, which is pivotably attached to the second rod 2, to the first curvedzone 9. A second finger part 11 is defined as the part which extendsfrom the first curved zone 9 to the free end 6 of the finger. Viewedfrom the first finger ends 5 to the free second finger ends 6, thefingers 4 bend in the first curved zone 9 away from the longitudinalcentre line 3. The outer guide 52, which here is essentially nothingother than the aforementioned annular outer guide 37, is provided insuch a way that, in the second position, it grips on the outerlongitudinal side 8 of the second part of the fingers. It is thusensured that the fingers 4 are held together in the second position andcannot pivot outwards in an uncontrolled manner. The fingers can also beprevented from pivoting outwards in an uncontrolled manner in adifferent way, rather than by the outer guide, such as by the annularconfining edge 13.

According to a further, optional embodiment, the medical instrument isconfigured in such a way that, in the first position, the inner guide 51grips on the inner longitudinal side 7 of the first finger part 10. Itis thus achieved that the fingers are held outwards in the firstposition, and cannot inadvertently pivot inwards.

According to a further, optional embodiment, in the case of the medicalinstrument 100, the outer guide 52 grips, in the first position, on theouter longitudinal side 8 of the first finger part 10 of the fingers 4.It is thus achieved that the fingers 4 are prevented from furtheroutward pivoting in the first position. If the fingers 4 hold aprosthesis in place, this means that the prosthesis is prevented frombeing able to be inadvertently released as a result of the fingers 4pivoting outwards. If, in the first position, the inner guide 51similarly grips on the inner longitudinal side 7 of the first fingerpart 10 of the fingers 4, the fingers then lie entirely fixed inposition in the first position. They cannot then pivot either inwards oroutwards. In general here, in the first position, the outer longitudinalside 8 of the second finger part 11 of the fingers 4 will lie free fromthe outer guide.

As shown in FIG. 2B, in the second position, the inner guide 51 canoptionally grip on the inner longitudinal side 7 of the first fingerpart 10 and/or the second finger part 11 of the fingers 4. The fingersare therefore prevented, in the second position, from being able topivot further radially inwards. If the fingers are further preventedhere by the outer guide from pivoting outwards, the fingers lie entirelyconfined in the second position, so that they are immovable in thesecond position. The fingers are thus prevented, in the second positionof the medical instrument, from being able to come loose, which isundesirable as this may cause damage to the patient. It will be clearthat, if the inner guide 51 grips on the inner longitudinal side of theone of the first finger part 10 or the second finger part 11, the otherof the first 10 or second 11 finger part of the fingers 4 can lie freefrom the inner guide 51.

According to a further design, the first curved zone 9 optionally showsa curve of at least 30°, in particular a curve of at least 45°, such asa curve of 50° or more. As shown in FIG. 2A, the curve in the firstcurved zone 9 is even more than 70°. The greater this curve, the morethe range X of the fingers will increase in relation to the length ofthe fingers, viewed in the direction of the longitudinal centre line 3.Here, the first finger part 10 can then run relatively close along thelongitudinal centre line 3, whereas the second finger part 11, inparticular the free finger ends 6, lie significantly further away fromthe longitudinal centre line.

According to a further embodiment, the fingers optionally show a kinkedshape in the first curved zone 9, at least on the inner longitudinalside 7 of the fingers 4. A kinked shape of this type, in particular incombination with a locally substantial bearing away of the inner guide51 in the direction of the longitudinal centre line 3, makes it possiblethat the fingers, from a specific time when there is little or nofurther shifting of the rods in relation to one another in thelongitudinal direction of the longitudinal centre line 3, may quicklyvary in span X.

According to a further embodiment, the inner guide 51 and the outerguide 52 are optionally immovable in relation to one another. In thecase of the applicator 100 according to FIGS. 1A, 1B, 2A and 2B, theinner guide 51 and the outer guide 52 are immovable in relation to oneanother.

It is noted that the previously discussed slot bases 36 form theproximal part of the inner guide 51. The distal part of the inner guidethen extends even further here within the area protected by the sleeve38.

The outer guide 52 has, in particular, a diameter smaller than the innerdiameter of the prosthesis 40. It is thus ensured that, following thedetachment and possible complete attachment and implantation of theprosthesis 40, the applicator 100, or at least the distal end part Ythereof, can be retracted in the proximal direction through theprosthesis.

FIGS. 3A and 3B show a second embodiment of a medical instrument 200according to the first aspect. This medical instrument is also intendedas an applicator for the implantation of a similar type of prosthesis 40as discussed in the embodiment according to FIGS. 1A and 2B. In thesecond embodiment as shown in FIGS. 3A and 3B, the same referencenumbers and symbols are used for corresponding items as in the firstembodiment according to FIGS. 1A, 1B, 2A and 2B. From the secondembodiment according to FIGS. 3A and 3B, only a distal part of themedical instrument is shown. The proximal part which is not shown may bedesigned in the same manner as in the embodiment according to FIGS. 1A,1B, 2A and 2B.

The main difference between the second embodiment according to FIGS. 3Aand 3B, and the first embodiment according to FIGS. 1A, 1B, 2A and 2B isthat the plurality of fingers 4 in the embodiment according to FIGS. 3Aand 3B is designed differently. To distinguish the plurality of fingersfrom this second embodiment shown in FIGS. 3A and 3B from the pluralityof fingers from the first embodiment according to FIGS. 1A, 1B, 2A and2B, the plurality of fingers 4 according to the second embodiment isdesignated by the term ‘third plurality of fingers’, and the differentreference number 144 is used therefor. As evident from FIGS. 3A and 3B,this does not therefore mean that a first and/or second plurality offingers must also be present.

Although there is no difference in content, but only a difference inrepresentation, the support ring 39 is shown in the second embodimentaccording to FIGS. 3A and 3B in a condition in which said support ringacts as a stop for the proximal side of the prosthesis 40.

Just as in the first embodiment according to FIGS. 1A, 1B, 2A and 2B,the fingers 144 in the second embodiment according to FIGS. 3A and 3Balso have a first finger end 5 pivotably attached to the second rod 2,and a free finger end 6. Furthermore, the fingers 144 of the thirdplurality of fingers also have a first curved zone 9. The fingers 144 ofthe third plurality of fingers are oriented in such a way that thepivotable attachment to the second rod 2 is located proximally from thefree finger ends 6, viewed from the perspective of the operator. Thefingers 144 of the third plurality of fingers therefore extend inrelation to the first plurality of fingers 4 according to the firstembodiment in the opposite direction. The fingers 144 of the thirdplurality of fingers furthermore project inside along the prosthesis 40in order to grip from within via a hook 60 on the distal flange feet 44at the distal end thereof, viewed from the perspective of the operator.

By then shifting the second rod 2 in relation to the tube 1 in thedistal direction, viewed from the perspective of the operator, the hooks60 fall free from the distal flange feet 44. In order to ensure herethat the fingers 144 of the third plurality of fingers are held togetherin the condition shown in FIG. 3B with a smaller span, an elastictensioning ring 62 (shown in FIG. 3B), such as a spring or an elastic,may optionally be provided. As shown in FIG. 3B, the span X, followingthe detachment of the prosthesis 40, is smaller than the diameter of theprosthesis 40. As further indicated by the arrow S and broken lines, thedistal flange feet, after they have been released by the fingers 144,can be flipped or bent over from the axial extended position to a radialposition.

The medical instrument according to the second embodiment as shown inFIGS. 3A and 3B offers the advantage that it takes up little space onthe distal side of the prosthesis 40, viewed from the perspective of theoperator. This medical instrument 200 is therefore very suitable ifthere is no space available in the patient on the distal side of theprosthesis.

FIG. 4 shows a third embodiment of a medical instrument 300 according tothe first aspect. This medical instrument 300 is also intended inparticular as an applicator for a prosthesis 80. This prosthesis 80 isof a type similar to that of the prosthesis 40 from FIGS. 1A, 1B, 2A,2B, 3A and 3B. The main difference is that, in the case of theprosthesis 80, not only the distal flange feet 82 but also the proximalflange feet 81 are bendable from an axial extended position to a radialposition (not shown in FIG. 4 ). In the third embodiment as shown inFIG. 4 , the same reference numbers and symbols are used forcorresponding items as in the first and second embodiment according toFIGS. 1A, 1B, 2A and 2B. From the third embodiment according to FIG. 4 ,only a distal part of the medical instrument is in turn shown. Theproximal part which is not shown may be designed in the same manner asin the embodiment according to FIGS. 1A, 1B, 2A and 2B.

The medical instrument 300 according to the third embodiment is similarto some extent to the medical instrument 200 according to the secondembodiment. The main difference compared with the medical instrument 200according to the second embodiment, is that, in the case of the medicalinstrument 300 according to the third embodiment, the fingers 144 of thethird plurality of fingers do not project inside through the prosthesis,but run outside along the prosthesis. For this purpose, the fingers 144of the third embodiment are modified compared with the fingers 144according to the second embodiment essentially in the hooks 60 (of thesecond embodiment). Instead of hooks 60, the fingers 144 are extendedhere by means of a second curved zone 70 in the distal direction, viewedfrom the perspective of the operator. The extended part 71 forms aso-called gripping section, with which the fingers grip outside aroundthe prosthesis 80 in order to overlap both the proximal flange feet 81and the distal flange feet 82 from outside and hold them in the extendedposition, thereby ensuring that the proximal and distal flange feet 81,82 can only return to a radial position after they have been released bythe fingers 144.

A further difference is that the tube 1 is provided with a cylindricalcarrier part 28 with slots 83 therein, through which the fingers 144 inthe position shown in FIG. 4 can project outwards. If the prosthesis 80has been detached, the fingers 144 pivot according to the arrow Wradially inwards and come (not shown) to lie entirely within the carrierpart 28 against the contact surface 117. This carrier part 28 istherefore a slotted element 34 as discussed in the first embodiment withreference to FIGS. 1A, 1B, 2A and 2B. In order to cause the fingers 144to move reliably to the reduced-span condition, an elastic tensioningring (not shown in FIG. 4 ) can be provided, corresponding to the secondembodiment according to FIGS. 3A and 3B.

In order to hold in place the prosthesis 80 carried on the distal lowerend of the carrier part 28 if the third plurality of fingers 144 isdrawn upwards in the proximal direction, the carrier part 28 can beprovided at the distal end, viewed from the perspective of the operator,with cams (not shown) projecting radially outwards, which project intoan intermediate space 83 between adjacent proximal flange feet 81.

In a manner corresponding to that described with reference to FIGS. 1A,1B, 2A and 2B, the tube 1 can be shifted in relation to the second rod 2in the proximal direction, viewed from the perspective of the operator,in such a way that the gripping sections 71 of the fingers 4 first cometo lie proximally from the distal flange feet 82 and, with furtherproximal retraction, also come to lie proximally from the proximalflange feet 81. It is thus possible to allow first the distal flangefeet 82 to bend round to a radial position and only thereafter theproximal flange feet 81. It is noted that it may also be possible forthe proximal flange feet 81 to change already in advance to the radialposition. In this case, the proximal flange feet will project throughbetween adjacent fingers 144 and no longer need to be bent to a radialposition.

In order to prevent the second rod 2 from being able to be pushed toofar in the distal direction out of the tube 1, a retainer plate 84 isprovided on the underside of the carrier part 28.

An applicator as shown in FIG. 4 is not only usable for implanting aso-called ‘prosthesis of the type with a tubular element’, but can alsobe used for other types of prostheses, such as a compressible and/orexpandable prosthesis or device, for example a stent.

FIGS. 5A-5C show a fourth embodiment of a medical instrument 400according to the first aspect. The medical instrument 400 is used hereas an applicator for a stent 90. This stent 90 may be provided on theinside or otherwise with a biological or artificial valve prosthesis,which can expand from a compressed condition when the stent expands. Thestent 90 may therefore optionally also be a so-called ‘valved stent’.With reference to the previously described embodiments of a medicalinstrument according to the first aspect, corresponding items are againdenoted here with corresponding reference numbers and symbols. From thefourth embodiment according to FIGS. 5A-5C, only a distal part of themedical instrument is in turn shown. The proximal part which is notshown may be designed in the same manner as in the embodiment accordingto FIGS. 1A, 1B, 2A and 2B.

The embodiment as shown in FIGS. 5A-5C is a double-headed embodiment.This applicator 400 has a distal ‘head’ with a first plurality offingers 4 and a proximal ‘head’ with a second plurality of fingers 94.The first plurality of fingers 4 and the second plurality of fingers 94are designed as mirror images of one another and have free finger ends 6pointing towards one another and first finger ends 5, which are attachedin a hinged manner, facing away from one another. The fingers 4 of thefirst plurality of fingers and the fingers 94 of the second plurality offingers both have a gripping section 71 and can jointly grasp the stent90 from opposite sides.

FIG. 5A shows the applicator 400 in a condition with the stent 90mounted thereon in the compressed condition. This is also the conditionof the stent and the applicator 400 when the stent is delivered to theintervention location in the patient. Having arrived at the interventionlocation, the fingers 4 of the first plurality of fingers and thefingers 94 of the second plurality of fingers are capable of pivotingoutwards from the first position shown in FIG. 5A to a wider positionshown in FIG. 5B, referred to here as the second position. Thus, thefingers 4 of the first plurality of fingers and the fingers 94 of thesecond plurality of fingers can jointly accompany the expansion of thestent 90 to the expanded condition shown in FIG. 5B. Displacement of thehinged attachments of the first finger ends of the first plurality offingers 4 and the second plurality of fingers 94 is not yet necessaryhere.

In order to be able to displace the first plurality of fingers 4 and thesecond plurality of fingers 94 in relation to the stent 90 and also inrelation to one another, the medical instrument is constructed fromthree rods, 1, 2 and 91, which are movable in relation to one another.The first rod 1 may be designed here as a tube in which both the secondrod 2 and the third rod 91 are housed in such a way that they arereciprocally displaceable in the longitudinal direction of the medicalinstrument. Here, the second rod 2 carries the first finger ends 5 ofthe first plurality of fingers 4 via a hinged attachment. The third rod91 carries the first finger ends 5 of the second plurality of fingers 94via a pivoting attachment. The fingers 94 of the second plurality offingers project via slots 93 outside the first rod 1.

As shown in FIG. 5C, the stent 90 can be released from the expandedcondition shown in FIG. 5B by, on the one hand, shifting the firstplurality of fingers 4 in relation to the stent 90 in the distaldirection D and, on the other hand, by shifting the second plurality offingers 94 in relation to the stent 90 in the proximal direction P.These shifts of the first plurality of fingers 4 and the secondplurality of fingers 94 can take place independently from one another,but a linked movement can also take place, wherein they are shiftedsimultaneously, to the same extent or otherwise.

As soon as the first and second fingers 4, 94 no longer overlap thestent 90, viewed in the direction perpendicular to the longitudinalcentre line 3, the first and second fingers 4, 94 can be pivoted to thenarrower position shown in FIG. 5C. This pivoting can take place in amechanically controlled manner or automatically, for example, if, in amanner comparable with the elastic tensioning ring 62 shown in FIGS. 3Aand 3B, a resilient element is provided around the first plurality offingers 4 or second plurality of fingers 94. However, the resilience ofa tensioning element of this type will be less than the force generatedduring the expansion of the stent 90, as the expansion of the stent 90would otherwise be hindered.

If the angle of inclination of the inner guide 51 in relation to thelongitudinal centre line 3 is made smaller, it is even possible here forthe free finger ends 6 of the first plurality of fingers 4 to dip viathe slots 92 into the sleeve part 195 on the distal end of the first rod1. This eliminates the risk of the free ends 6 of the first plurality offingers 4 being able to damage tissue of the patient when the applicatoris retracted in the proximal direction P. This is less important for thefree ends 6 of the second plurality of fingers 94, as they point duringthe retraction in a direction opposite to the direction of retraction P.However, in the condition shown in FIG. 5C, these free ends 6 can alsodip if required inside into the sleeve part 195 by extending the slots93 on the underside by shortening the sleeve part 195 in the region of96.

In the case of stents, they are normally delivered to the interventionlocation in a sleeve. The sleeve is then withdrawn in situ and the stentexpands. If the stent is not positioned at precisely the correctlocation and the sleeve has already been withdrawn (too far), the stentcan then no longer be repositioned. Retrievable stents are in factknown, but once the sleeve has been withdrawn too far, it is difficultor impossible to correct this situation. The advantage of the applicatoraccording to FIGS. 5A-5C and also the applicator still to be discussedaccording to FIGS. 6A-6C is that stents can be implanted herewith in amanner which to a large extent allows for correction. In any event, thepivotable fingers make it possible, following expansion of the stent,for the stent to be compressed once more and for the stent to beentirely removed or repositioned. In addition thereto, but also entirelyseparately therefrom, the pivotable fingers enable the stent expansionto be carried out in an extensively and particularly controlled manner.

FIGS. 6A-6D show a fifth embodiment of a medical instrument 500according to the first aspect. This medical instrument is also intendedas an applicator, in this case an applicator for a stent or so-called‘valved stent’. With reference to the previously described embodimentsof a medical instrument according to the first aspect, correspondingitems are again denoted here with corresponding reference numbers andsymbols. From the fifth embodiment according to FIGS. 6A-6D, only adistal part of the medical instrument is in turn shown. The proximalpart which is not shown may be designed in the same manner as in theembodiment according to FIGS. 1A, 2B, 2A and 2B.

The prosthesis is denoted in FIGS. 6A-6D by reference number 96 and canbe distinguished from the prosthesis 90 shown in FIGS. 5A-5C inparticular by a ‘prosthesis of the type with a tubular element’separately disposed hereon or integrated herewith, as described inpreviously repeatedly mentioned PCT applications of the inventor. Aprosthesis such as the prosthesis 96 has a tubular configuration andcomprises a tubular part 198 with proximal flange feet 83 and distalflange feet 82 provided thereon. Of these flange feet, at least thedistal flange feet 82 can be moved from an axial position to a radialposition. In the case of the fifth embodiment according to FIGS. 6A-6D,the proximal flange feet 83 can also be moved from an axial position toa radial position 83. The prosthesis 96 is then attached to surroundingtissue then by clamping tissue between the proximal flange feet 83 anddistal flange feet 82 and/or by anchoring the proximal flange feet 83and/or distal flange 82 in surrounding tissue.

The medical instrument 500 according to the fifth embodiment differsfrom the medical instrument 400 according to the fourth embodimentparticularly in the sense that the free ends 6 of the first plurality offingers 4 and the second plurality of fingers 94 are provided withgripping elements 95. These gripping elements 95 are formed here as acentral slot 97 with a gripping part on either side, i.e. an innergripping part 98 and an outer gripping part 99. The gripping parts 98and 99 can run roughly parallel. In this embodiment, the inner grippingpart 98 on the inside of fingers 4 and 94 is in each case shorter thanthe outer gripping part 99 on the outside of the fingers 4 and 94. It isnoted that the inner gripping part 98 and the outer gripping part 99 maypossibly also be of equal length.

With reference to FIG. 6A, the proximal flange feet 83 and the distalflange feet 82 are accommodated in the initial condition in the slots 97of the gripping elements 95 of the second plurality of fingers 94 andthe first plurality of fingers 4 respectively.

By designing the gripping parts 99 of the gripping elements 95 locatedon the outside as sufficiently long (and, in addition, possibly theslots 97 of the gripping elements 95 as sufficiently deep), viewed inthe longitudinal direction of the longitudinal centre line 3, the firstplurality of fingers 4 and the second plurality of fingers 94 arecapable, in a manner corresponding to that shown in FIGS. 5A-5C ofaccompanying the expansion of the prosthesis 96, but without releasingthe proximal flange feet 83 and the distal flange feet 82. This is shownin FIG. 6B, where an expanded prosthesis 96 is shown, the proximalflange feet 83 and the distal flange feet 82 of which are still held inplace by the gripping elements 95.

The first plurality of fingers 4 and the second plurality of fingers 94are then displaced in relation to the prosthesis 96 in a mannercorresponding to that shown in the embodiment according to FIGS. 5A-5Cin such a way that the distal flange feet 82 and proximal flange feet 83are released. The condition thus reached is shown in FIG. 6C.

The distal flange feet 82 and the proximal flange feet 83 can then movefrom the axially extended position to the radial position for anchoringin and/or on surrounding tissue. This condition is shown in FIG. 6D.

As can furthermore be seen in FIGS. 6C and 6D, the free ends 6 of thefirst plurality of fingers 4 dip via the slots 92 into the tube part 95(corresponding to the manner described in FIG. 5C but now actuallyshown).

The embodiment according to FIGS. 6A-6D is suitable in particular forimplanting a so-called ‘valved stent’. As shown in FIGS. 6A-6D,sufficient space in fact remains centrally in the prosthesis 96 toaccommodate the valve flaps and commissures of a valve. The central partof the applicator extending through the prosthesis 96 can in fact bedesigned as very slim. It should be clear that the embodiment as shownin FIGS. 6A-6D is suitable not only for implanting a stented valveprosthesis, but also for implanting a conventional stent which isprovided for anchoring in surrounding tissue or is integrated with a‘prosthesis of the type with a tubular element’ as described in detailin earlier PCT applications of the inventor.

The great advantage of the applicator according to FIGS. 6A-6D is that astent can be implanted herewith with anchoring elements mounted thereon,wherein the stent can first be allowed to expand and only thereafter canthe anchoring elements be released to be anchored in surrounding tissue,such as the annulus of a heart valve. The anchoring elements can thus beprevented from moving prematurely to an anchoring position and therebyno longer being able to be anchored firmly in the surrounding tissue oreven no longer being able to be anchored at all.

FIGS. 7A-7C show very schematically a medical instrument 600 accordingto a sixth embodiment. This medical instrument is shown here as anapplicator for an expandable stent 90. FIG. 7A shows the medicalinstrument 600 and the stent 90 in a compressed condition, FIG. 7B showsthe stent 90 and the medical instrument 600 in an expanded condition,wherein the stent 90, however, has not yet been detached, and FIG. 7Cshows the medical instrument 600 and the stent 90 in a condition afterthe stent 90 has been expanded and detached. With reference to thepreviously described embodiments of a medical instrument according tothe first aspect, corresponding items are again denoted here withcorresponding reference numbers and symbols. From the sixth embodimentaccording to FIGS. 7A-7C, only a distal part of the medical instrumentis in turn shown. The proximal part which is not shown may be designedin a manner comparable with the embodiment according to FIGS. 1A, 1B, 2Aand 2B.

The main difference compared with the previously described embodiments,in particular the fourth embodiment according to FIGS. 5A-5C and thefifth embodiment according to FIGS. 6A-6D is that the fingers of thefirst plurality of fingers 4 and the second plurality of fingers 94 arenot pivotable here. The displacement of the fingers 4 and 94 isimplemented here by means of a translation along a surface which liesobliquely in relation to the longitudinal centre line 3. The firstplurality of fingers 4 and the second plurality of fingers 94 can thus,to a substantial extent, precisely accompany the expansion of the stent90 to virtually the outer expansion position of the stent without beinghindered therein by surrounding tissue. It should be clear in thiscontext that the gripping sections 71 of the fingers 4 and 94 are shownhere as exaggeratedly thick and, viewed in a direction perpendicular tothe longitudinal centre line 3, may therefore be designed as muchthinner.

As shown in FIGS. 7A-7C, this mobility of the fingers 4 and 94 isachieved by providing the second rod 2 with a first conical guidesurface 101 and by providing the first plurality of fingers 4 at thefirst finger ends 5 with a guide part 102 which is shiftable along andin contact with the first conical guide surface 101 in order to displacethe fingers 4 from a first position to a second position, wherein thedistance from the guide parts 102 to the longitudinal centre line 103differs in the first position and the second position. In acorresponding manner, the third rod 91 is provided with a second conicalguide surface 103. The fingers 94 of the second plurality of fingers arein turn provided in a corresponding manner at a first finger end 5 witha guide part 102 which is shiftable along and in contact with the secondconical guide surface 103 from a first position to a second position.The conical guide surfaces 101 and 103 face towards one another here,and the free ends 6 of the first plurality of fingers 4 and the freeends 6 of the second plurality of fingers 94 similarly face towards oneanother.

With regard to the medical instrument 600 as shown in FIGS. 7A-7C, it isnoted that, from the first plurality of fingers 4 and the secondplurality of fingers 94, only one finger with the associated guide part102 is shown in each case. The purpose of this is to maintain clarity inFIGS. 7A-7C. In practice, the first plurality of fingers 4 and thesecond plurality of fingers 94 will each consist of a plurality offingers disposed in a distributed manner around the longitudinal centreline 3. From a practical point of view, the number of fingers perplurality will be at least three. In practice, this will normally beexpected to be 4, 5, 6, 7, 8, 9, 10, 11 or 12.

Although the gripping sections 71 and the guide part 102 of a respectivefinger will normally be rigid, i.e. immovable, in relation to oneanother, it is also optionally possible for the gripping sections 71 tobe designed as pivotable in relation to the guide part 102. For example,as described earlier with reference to FIGS. 1A, 1B, 2A, 2B, 3A, 3B, 4,5A-5C, and 6A-6D.

The first plurality of fingers 4 can optionally be interconnected bymeans of a resilient tensioning ring 62 which extends around thelongitudinal centre line 3 and is otherwise comparable with thetensioning ring 62 as shown in FIG. 3B in order to hold them in positionon the medical instrument. However, this can also be done in a differentmanner with the aid of different means.

Once the medical instrument and the stent 90, in the compressedcondition, as shown in FIG. 7A, have arrived at the interventionlocation, the stent 90 can then be expanded in a completely controlledmanner by pressing the second rod and the third rod towards one another,as a result of which the reciprocal interval Q1, as shown in FIG. 7A,between the conical surfaces 101 and 103, decreases to Q2, as shown inFIG. 7B. The two tensioning rings 62 are thereby stretched and hold thefirst plurality of fingers 4 and the second plurality of fingers 94positioned as such on the instrument, but at a greater distance from thelongitudinal centre line 3.

Once the stent 90 has then sufficiently or completely expanded, thesecond rod 2 and the third rod and 91 can again be drawn out from oneanother in order to increase the distance Q2 to the distance Q3, asshown in FIG. 7C. The gripping sections 71 of the first plurality offingers 4 and the second plurality of fingers 94 will thereby bedetached from the stent 90. The tensioning rings 62 will then ensurethat the first plurality of fingers 4 and the second plurality offingers 94 move from the wide position shown in FIG. 7B to theconstricted position shown in FIG. 7C, wherein said constricted positionmay even have a smaller span Q3 than in the initial condition accordingto FIG. 7A. The medical instrument 600 can then be removed from thepatient through the stent 90.

Although the medical instrument 600 according to the sixth embodimenthas been described on the basis of a double-headed design, it will beclear that it may also be designed with one single plurality of fingers,i.e. the first plurality of fingers 4 or the second plurality of fingers94. Thus, it will, for example, be clear that the embodiment accordingto FIGS. 1A, 1B, 2A and 2B can in fact easily be implemented by means ofa plurality of fingers 4 corresponding to the sixth embodiment shown inFIGS. 7A-7C and that the embodiments according to FIGS. 3A, 3B, 4, 5A-5Cand 6A-6D can also be implemented with one conical surface per pluralityof fingers and fingers corresponding to the design according to FIGS.7A-7C.

FIGS. 8A and 8B show a medical instrument 700 according to a seventhembodiment of the first aspect. This medical instrument 700 is, inparticular, suitable as an applicator for a ring prosthesis 800according to the second aspect of this application. Further details ofthis ring prosthesis can be found in FIGS. 9A and 9B, which shows afirst design of the ring prosthesis according to the second aspect. Toavoid misunderstanding, it is, however, noted that, in the ringprosthesis in FIGS. 9A and 9B, the pins 801 are provided on the outsideof the ring prosthesis, whereas the pins of the ring prosthesis in FIGS.8A and 8B are provided on the inside of the ring prosthesis. However,the instrument 700 is also very readily usable for the ring prosthesisas shown in FIGS. 9A and 9B without this instrument 700 requiring anyadaptation for this purpose.

With reference to the previously described embodiments of a medicalinstrument according to the first aspect, corresponding items are againdenoted here with corresponding reference numbers and symbols. From theseventh embodiment according to FIGS. 8A and 8C, only a distal part ofthe medical instrument is in turn shown. The proximal part which is notshown may be designed in the same manner as in the embodiment accordingto FIGS. 1A, 1B, 2A and 2B.

The medical instrument 700 comprises a first rod 1 in the form of a tubewith a second rod 2, shiftable in relation to the tube 1, housedtherein. The second rod 2 is provided with a conical surface at itsdistal end, viewed in relation to the apparatus. This conical surface isnot visible in FIGS. 8A and 8B, but does not differ per se in design andoperation from the conical surface 103 shown in FIGS. 7A-7C. Fingers 4are supported on the conical surface of the second rod in the same wayas the fingers 94 are supported on the conical surface 103 in FIGS.7A-7C. The tube 1 is provided with slots 106, in which the fingers 4 areguided axially, and which hold the fingers 4 in their place. In the sameway as the fingers 94, the fingers projecting outwards from the slots106 have a free, second end 6 and a first end with an oblique surface,so that the fingers 4 can shift along the conical surface of the secondrod in the event of axial displacement of the second rod in relation tothe fingers 4. In addition to fingers 4, the medical instrument alsofurther comprises fingers 855. These fingers 855 can possibly be mountedimmovably on the tube 1. In order to be able to reduce the span of thedistal end of the instrument 700, for example in order to facilitate thedelivery to the intervention location, it is desirable for the fingers855 to be movable in a radial direction in order to be able to retractthem in a radially inward direction and/or to project them furtheroutwards in a radially outward direction. This can be implemented in themanner described earlier in relation to the first aspect, for example bymeans of a third rod with a conical surface which interworks with anoblique surface on the inside of the fingers. This third rod may bedesigned as a tube and may lie between the first and second rod, but itmay also be located in the second rod, if the second rod is designed asa tube. If the tube 1 needs to be held fixed in relation to theintervention location and the prosthesis also needs to be able to bepushed away in the distal direction, it is then expedient if the fingers855 are guided in axial slots which are formed in the tube 1.

With reference to FIGS. 9A and 9B, the ring prosthesis 800 is formedfrom a wire 802 which extends along a waved pattern in thecircumferential direction as a waved (first) ring. As shown withreference to FIG. 9A, the waved ring in this example has twelve wavepeaks 804 and twelve wave troughs 803. Each wave peak 804 carries a pin801 which extends in the direction of the axial centre line 805 of thering prosthesis 800. As a result of the waved pattern, this ringprosthesis can be reduced in diameter or, conversely, increased indiameter. In the case of a reduction in the diameter, adjacent wavepeaks 804 and adjacent wave troughs 803 will come to lie closer to oneanother. In the case of an increase in the diameter, adjacent wave peaks804 and adjacent wave troughs 803 will come to lie further away fromanother. The wave length L, viewed in the circumferential direction ofthe ring, will therefore decrease in the event of a reduction in thediameter, whereas the wave height H will, conversely, increase in theevent of a reduction in the diameter. Conversely, in the event of anincrease in the diameter, the wave length L will increase and the waveheight H will decrease.

If the ring prosthesis 800 is loaded onto the applicator 700 shown inFIGS. 8A-8C, the fingers 4 (see FIG. 8A) will move with their free endsfrom the inside against the peak 804 of the wave. The pins attached tothe waved ring 802 at the midpoint of the peak 804 (see the pin 444indicated for this purpose by broken lines on the left in FIG. 8A, whichpresents a pin from the ring prosthesis shown in FIGS. 9A and 9B) willthen, as shown in FIG. 8A with the dashed-line pin 444, lie against theoutside 108 of the free end 6 of a finger 4. If the ring prosthesis sitshigher on the fingers 4, the pin 444 will no longer project under theaxial outer edge 108 of the finger 4 and therefore be protected from theenvironment by the axial outside 108 of a finger 4. A pin 444 can thusbe prevented from prematurely being able to prick into tissue or beingable to remain caught up in tissue if the applicator, or at least thedistal end thereof, viewed from the perspective of the operator, ismoved through the patient to the intervention location. If the pin 444bends radially inwards in its final position, it is advantageous if abend of this type can be temporarily held in place by the axial outside108 of the finger 4. In the case of the ring prosthesis as shown inFIGS. 8A-8C, the pins lie on the inside of the ring prosthesis, as aresult of which the risk of them remaining caught up in tissue orpricking prematurely into tissue during the delivery to the interventionlocation is much smaller. In this case, it is advantageous if thefingers 855 are extended distally on the underside thereof, saidextension not being shown in this drawing, in such a way that anextension of this type lies in the longitudinal direction along theinside of the pin 801, in order to prevent this pin 801 temporarily frombending radially inwards. A distal extension of this type of the finger855 could then be disposed at some distance from the periphery of thefinger 855, so that the underside of the periphery of the finger 855 canmaintain contact from above with the upper side of the ring. In thiscase, the fingers 4 may also have a peripheral extension which gripsfrom above on the ring. Implantation of the ring will then be such that,due to the distal displacement of the fingers 4, the ring is displaceddistally, wherein the distal extensions of the fingers 855 act as aguide for the pins 801. As soon as these pins 801 no longer have contactwith these distal extensions of the fingers 855, the pins 801 maypossibly bend in a radially inward direction.

During the delivery to the intervention location, the waved ring 802stretched out on the applicator 700 may have a smaller diameter thanshown in FIG. 8A. The second rod 2 will then be retracted in a proximaldirection in relation to the fingers 4. The waved ring can therefore bedelivered more easily to the intervention location in the patient in acondition with a relatively smaller diameter, in particular if narrowpassages must be passed through. The risk of the free ends of the pins801 of the ring 802 inadvertently damaging tissue or remaining caught uptherein during the delivery to the intervention location can thereforealso be (further) reduced.

If the ring 802 is delivered to the intervention location in thereduced-diameter condition, the ring can be modified there to therequired diameter by expanding it by means of the fingers to thecondition shown in FIG. 8A, by shifting the second rod 2 in the distaldirection in relation to the fingers 4/tube 1. It is noted that it isalso possible to deliver the ring 802 to the intervention location inthe expanded condition shown in FIG. 8A.

Having arrived at the intervention location, the fingers 4 can beretracted in a radial direction by retracting the second rod 2 in theproximal direction P in relation to the fingers. As shown in FIG. 8B,the fingers 4 then come to lie free from the waved wire 802.Subsequently (or simultaneously with or prior to the radial retractionof the fingers 4), the ring prosthesis can be pushed down in the distaldirection D by means of the fingers 855 in order to drive the pins 801(or 444) into tissue, such as valve annulus tissue). Once the ringprosthesis is attached to the tissue, the instrument 700 can beretracted in the proximal direction, as shown in FIG. 8C.

In the case of a ring prosthesis according to FIGS. 9A and 9B, the pins444, from the time that they come free from the outsides 108 of thefingers 4, if the pins 444 are pre-tensioned for this purpose, will,corresponding to arrow Z (FIG. 8C) pivot inwards over a shorter orlonger distance. The inwardly-pivoted condition can be seen in FIG. 9B(and FIG. 8C, to the left of the dashed-line pin 444). The anchoring inthe tissue is thus improved and the risk of the ring prosthesis comingloose from that tissue is reduced. In order to prevent the pins 444 fromprematurely pivoting inwards here, the fingers 4 will possibly beretracted radially only after the ring prosthesis has been attached inthe tissue.

FIGS. 10A and 10B show a medical instrument 900 according to an eighthembodiment of the first aspect. This medical instrument 900 is, inparticular, suitable as an applicator for a ring prosthesis 1000according to a further aspect of this application. Further details ofthis ring prosthesis can be found in FIG. 11A and FIG. 11B, which showsa second design of the ring prosthesis according to the second aspect.With reference to the previously described embodiments of a medicalinstrument according to the first aspect, corresponding items are againdenoted here with corresponding reference numbers and symbols. From theeighth embodiment according to FIGS. 10A and 10B, only a distal part ofthe medical instrument is in turn shown. The proximal part which is notshown may be designed in the same manner as in the embodiment accordingto FIGS. 1A, 1B, 2A and 2B.The applicator 900 is designed in virtually the same way as theapplicator as shown in FIGS. 1A, 1B, 2A and 2B. The difference lies inthe shape of the fingers 904, which is different from that of thefingers 4 in FIGS. 1A, 1B, 2A and 2B. The difference in shape is thatthe fingers 904 continue at 906 in a radial, outward direction, whereasthe fingers 4 in FIGS. 1A, 1B, 2A and 2B continue there roughly parallelto the longitudinal centre line 3 to come to a point. The fingers 904have a recess 905 at their free ends 6 in order to grip on a prosthesis,in this case the ring prosthesis 1000.

The ring prosthesis 1000 is formed, just as the ring prosthesis 800,from a wire 802 which has a waved pattern of wave troughs 803 and wavepeaks 804. The ring prosthesis 1000 also has pins 801 for anchoring intissue. However, in the case of the ring prosthesis, the pins 801 areattached to the wave troughs 803. This offers the advantage that, if thepins 801 are pricked into the annulus tissue of a valve, the remainderof the ring prosthesis 1000 will lie essentially outside the passagethrough which blood flows. The waved wire 802 may rest on the annulus. Afurther difference is that the ring prosthesis 1000 is provided withring segments 806. In a first condition, adjacent ring segments 806 lieat a distance from one another. In a second condition with a smallerdiameter, these ring segments 806 may lie with their ends against oneanother, thereby defining a minimum diameter for the ring prosthesis1000. Thus, this ring prosthesis cannot further narrow beyond thisminimum diameter. A completely different function of the ring segmentsis that they can serve to support a further prosthesis which is to beimplanted in or near the ring prosthesis and/or to affix a furtherprosthesis of this type. The limiting function with regard to theminimum diameter may even be dispensed with in this support/attachmentfunction, or the ring segments do not in fact have to be provided insuch a way that they can form an essentially closed second ring. It isnoted that the ring segments are optional in the case of the ringprosthesis, and may therefore also be absent, and that, if required,ring segments 806 of this type may also be provided in the ringprosthesis 800.

Just as in the ring prosthesis 800, the pins 801 can pivot inwards overa shorter or long distance. However, it is noted that in both the ringprosthesis 800 and the ring prosthesis 1000, the pins 801 can also pivotor bend in a different direction in order to improve the anchoring insurrounding tissue. A different direction of this type may, for example,be in a radially outward direction and/or in a tangential direction.Adjacent pins can also bend towards one another in both the ringprosthesis 800 and the ring prosthesis 1000 in order to form a clamptogether.

Returning to FIGS. 10A and 10B, it can be seen that the applicator 900can hold the ring prosthesis in place when the latter has a largerdiameter, as shown in FIG. 10A, as well as when the latter has a smallerdiameter. This diameter change can be imposed in a forced manner withthe aid of the applicator 900 by displacing the fingers from theposition shown in FIG. 10A to the position shown in FIG. 10B or viceversa by displacing the fingers from the position shown in FIG. 10B tothe position shown in FIG. 10A. The waved wire 802 makes it possible forthe ring prosthesis to vary in diameter here. Thus, it is possible, forexample, to deliver the ring prosthesis with a smaller diameter (FIG.10B) to the intervention location and to increase it in diameter therebefore attaching it to surrounding tissue. Separately herefrom or inaddition hereto, the applicator 1000 can also be used, after the ringprosthesis 1000 has been attached to the surrounding tissue, to force itto be reduced in diameter. After the ring prosthesis has been attachedto the surrounding tissue and has possibly been reduced in diameter bymeans of the applicator 1000, the ring prosthesis 900 can be detached byretracting the applicator in the proximal direction P.

FIGS. 12A and 12B show a third design of a ring prosthesis 1100according to the second aspect. FIG. 12A shows the ring prosthesis 1100in a perspective view from above with the clamping mouths (to bediscussed below) shown in the closed position and FIG. 12B in aperspective view from the side edge with the clamping mouths 807 (to bediscussed below), shown in schematised form, in a similarly closedposition. This ring prosthesis 1100 differs from the ring prostheses 800and 1000 in that the anchoring elements are clamping mouths 807 ratherthan pins 801. Each clamping mouth 807 comprises a first jaw part 808and a second jaw part 809 which is movable in relation to the first jawpart 808. In this design, the first jaw part 808 is immovable, andextends essentially parallel to the surface defined by the wavedpattern. The second jaw part 809 is shown in the more or less completelyclosed position, but is movable under the influence of a temperaturetreatment so that it can extend in the direction of the arrow C, in thedirection of the longitudinal axis across the ring, in order to attainan opened position. In the shown closed position, the second jaw part809 is tilted towards the first jaw part 808—the condition shown—inorder to clamp tissue between the first jaw part and the second jawpart. If the tissue to be clamped is thinner, the clamping mouths willclose even further than shown in FIGS. 12A and 12B. The clamping mouths807 are attached to the wave troughs 803 of the waved wire 802.Furthermore, the clamping mouths 807 are made from a memory material,such as a previously mentioned memory plastic or a previously mentionedmemory metal. In the design shown, the clamping mouths are made fromnitinol and, in FIG. 12A, are in the virtually closed condition. In theevent of further heating and exceeding of a threshold temperature, thesecond jaw parts 809 will then tilt, under the influence of apre-tension, even further towards the first jaw parts 808.

FIGS. 12A and 12B show the clamping mouths 807 as attached to the wavetroughs. If required, the clamping mouths can also be attached to thewave peaks. It is furthermore noted that, instead of both jaw parts 808and 809 being movable, it is also very readily possible for only the jawparts 808 or only the jaw parts 809 to be movable, while the other jawparts 809 and 808 respectively are immovable. Furthermore, the clampingmouths may, if required, be provided with teeth for better anchoring inthe tissue to be clamped in the clamping mouths. Furthermore, an openstructure of the clamping mouths, as can be seen in case of the clampingmouths 809 in FIG. 12A, can also contribute to an improved anchoring inthe tissue to be clamped.

FIGS. 13A and 13B show an applicator 1500 according to the fifth aspectof this application. This applicator 1500 is essentially constructedfrom four components, i.e. a tube 1501, a pin 1502, a sheathing 1505 anda carrier 1504. The pin 1502 is provided with an outer screw thread1507. This screw thread may extend over the entire length of the pin,but it generally suffices if this outer screw thread extends over only apart of the length. In order to be able to rotate the pin 1502 withease, said pin is provided on the proximal end with an operating button1503 which is connected in a rotation-resistant manner to the pin. Thepin 1502 projects into the tube 1501 and extends through the entirety ofthis tube so that it projects from the tube 1501 at both the proximalend and the distal end. The carrier 1504 is attached to the pin at thedistal end of the pin 1502. Here, the carrier 1504 is rotatable inrelation to the pin 1502 around the longitudinal centre line 1508 of thepin, so that, if the pin is rotated by means of the operating button1503, the carrier can be prevented from rotating with it.

The tube 1501 is provided at a given location with an inner screw threadwhich mates with the outer screw thread 1507. It can thus be achievedthat, when the pin 1502 rotates in relation to the tube 1501, the tubeand the pin move in an axial direction in relation to one another. Thetube 1501 is provided with a sheathing 1505 on the distal end. Thissheathing is attached to the tube 1501. This may be a rotation-resistantattachment, but an attachment rotatable around the longitudinal centreline 1508 is possibly also conceivable. When the pin 1502 is rotated—inthe correct direction—in relation to the tube 1501, the carrier 1504will slide inwards into the sheathing in the proximal direction P. Here,the axial guide 1507 prevents the carrier 1504 from rotating in relationto the sheathing 1505. The axial guide is designed here as a pin 1507which is shiftable through the bore 1511. However, this can also be donedifferently, for example by means of a rib on the inside of thesheathing which grips into a slot in the outside of the carrier 1504.

The carrier 1504 has a carrier surface 1510 facing radially outwards, onwhich the prosthesis can be attached. Here, a ring prosthesis is shownwhich is very similar to the ring prosthesis as shown in FIG. 8C. Themain difference is that, in FIG. 8C, the wave-shaped pattern is roughlyradially oriented, whereas the wave pattern in FIGS. 13A and 13B isalmost completely axially oriented. The ring prosthesis with the wavedwire 802 and pins 801 is clamped here on the carrier surface 1510.

As shown in FIGS. 13A and 13B, the outer contour of the carrier surface1510 is essentially the same as the inner contour of the sheathing 1505,so that the carrier surface can be accommodated more or less withoutplay in the sheathing.

If the carrier 1504 then slides inwards into the sheathing 1505, theprosthesis 801, the prosthesis 802 slides away from the carrier in thedistal direction.

In order to be able to insert the applicator easily through channels orpassages in the patient, the carrier is provided on the distal end witha nose part 1506 with a rounded point 1509.

The ring prosthesis according to the second aspect can be used for moreapplications than only the constriction of a dilated valve. Examples ofsuch other applications are:

-   -   The ring prosthesis according to the second aspect can be        integrated with a valve prosthesis comprising valve flaps. The        ring prosthesis can then draw the tissue from around the outside        against the valve prosthesis in order thereby to prevent leakage        outside along the valve prosthesis.    -   The ring prosthesis according to the second aspect can be used        as a support and/or mounting point for a valve prosthesis        comprising valve flaps. The ring prosthesis will then first be        implanted, followed by the valve prosthesis comprising valve        flaps. According to the second aspect, this application        therefore also relates to a method for carrying out a heart        valve repair, wherein a ring prosthesis according to the second        aspect is first implanted and thereafter a valve prosthesis is        attached to the implanted ring prosthesis. In a step preceding        these two steps, the old, diseased heart valve can first be        removed if it had not yet been removed.    -   The ring prosthesis according to the second aspect is also        usable as a closing system for closing an access port made in a        human or animal organ. When carrying out an intervention on the        heart, the surgeon may, for example, make an access port through        the heart wall. This is done, inter alia, at the apex. This        access port must be closed once more in order to prevent leakage        from the heart. This can be done by implanting a ring prosthesis        according to the second aspect around the port made in the heart        wall (such as at the apex) and then reducing the ring prosthesis        in diameter. The tissue is then drawn inwards and the port is        closed. The tightly drawn tissue can then usually expand once        more to result in a complete seal.

FIGS. 14A and 14B show a medical instrument 1200 according to a ninthembodiment of the first aspect. This medical instrument 1200 is suitablein particular for cutting away surrounding material or for punching apassage. FIGS. 14A and 14B show a double-headed design with a distalhead 1202 and a proximal head 1201. The distal head 1202 is designed onthe additional cutting means 1205, 1206 in the same way as the head fromFIGS. 1A, 1B, 2A and 2B. The proximal head 1201 is designed as themirror image of the distal head 1202, on the understanding that theadditional cutting means 1203, 1204, are designed differently. Withreference to the previously described embodiments of medical instrumentsaccording to the first aspect, corresponding items are again denotedhere with corresponding reference numbers and symbols. From the ninthembodiment according to FIGS. 14A and 14B, only a distal part of themedical instrument is in turn shown. The proximal part which is notillustrated may be designed in a manner comparable to the embodimentaccording to FIGS. 1A, 1B, 2A and 2B or FIGS. 5A-5C and 6A-6D.

The proximal head 1201 with the second plurality of fingers 94 carries acutting element 1203. The cutting element 1203 is designed as acylindrical part which is variable in diameter in order to be able toexpand from the position shown in FIG. 14A to the position shown in FIG.14B if the second plurality of fingers 94 are spread. The cuttingelement 1203 is designed in particular to be stretchable, such aselastically stretchable, in order to allow this expansion. This examplecan also be implemented by designing the cutting element 1203 as aspiral-type knife, formed, for example, from a plate material bent intoa spiral-type configuration. A spiral-type knife of this type will havetwo overlapping ends, viewed in the circumferential direction. In thecase of a smaller diameter, the overlap of the end parts will be greaterthan in the case of a larger diameter. The cutting element 1203 has acutting edge 1204, with which it can cut into tissue. This cutting canbe done by rotating the medical instrument 1200 around its longitudinalcentre line 3 and/or, in the manner of punching, by displacing thecutting organ 1203 in the distal direction D in relation to the materialto be cut. The cutting element 1203 is suitable, inter alia, forcreating or widening passages through a vascular wall or through othertissue, but can also be used to remove deposits or bulges on the insideof a vascular wall or organ, or to cut into or remove a diseased heartvalve. In the condition shown in FIG. 14A, the cutting element 1203lies, as it were, sunk into the medical instrument 1200, so that itcannot damage surrounding tissue. At the intervention location, thethird rod 91 can be displaced in the distal direction in relation to thefirst rod 1 which is designed as a tube in order to spread the fingersfrom the condition shown in FIG. 14A to the condition shown in FIG. 14B.

In the case of the distal head 1202, each finger 4 is provided with acutting edge 1205 on the radial outside. This cutting edge optionallyends at the free finger ends 6 in a sharp end 1206, in particular asharp point. Viewed from the free finger end 6, the cutting edge extendsover the entire area 1207 or a part thereof. The fingers 4 may alsooptionally have a cutting edge 1208 on the radial inside 1208 whichextends from the free finger end 6 over some distance in the directionof the finger end 5. In the condition shown in FIG. 14A, the cuttingedges 1205 and sharp ends 1206 of the fingers 4 lie sunk into theslotted element 34 or otherwise in the medical instrument 1200 so thatit cannot damage surrounding tissue. At the intervention location, thesecond rod 2 can be displaced in the proximal direction in relation tothe first rod 1, which is designed as a tube, in order to spread thefingers from the condition shown in FIG. 14A to the condition shown inFIG. 14B. The fingers 4 with cutting edges 1205 are usable to create orwiden a passage in a vascular wall or other tissue. The fingers 4 withcutting edges are also usable to remove deposits or bulges on the insideof a vascular wall or organ, or to cut into a diseased heart valve sothat it can be removed more easily.

To illustrate different designs, the medical instrument 1200 is shownwith differently designed heads 1201 and 1202. It will thus be clearthat, in the case of a double-headed design, the distal head 1202 andthe proximal head 1201 can both be designed in the same way, for exampleboth with a cutting element 1203 or both with cutting edges 1205 on thefingers. The advantage of a double-headed design is that tissue or othermaterial can be cut simultaneously or non-simultaneously from twoopposite sides. It is furthermore noted that both the cutting element1203 and cutting edges 1205 can also be very readily used in the case ofa single head. This may then be the proximal head 1201 or the distalhead 1202. If only a proximal head 1201 is provided with cutting means(in the absence of a distal head), it is possible to form a passagethrough tissue which was entirely closed prior to the intervention.

With reference to the medical instrument 1200, it is noted that, if theproximal head 1201 and the distal head 1202, at least in particular thefree finger ends of the fingers thereon, are placed closer to oneanother, the plurality of fingers on the one head can be used as ananvil which interworks with the plurality of fingers of the other headwhich are provided with cutting elements. Counter-pressure can then beapplied during the cutting. The finger ends may thereby overlap oneanother to produce a pincer effect. The fingers on both heads may alsobe provided here with cutting elements.

With reference to the various medical instruments shown above accordingto the first aspect of the application, it will be clear that they couldalso be used to measure the diameter of a passage or to measure thepressure of and/or tension and/or tissue resilience in tissuesurrounding a passage. By allowing the fingers to expand in a controlledmanner by means of the operating button and by providing a graduatedscale in the operating button, the rotation of the operating button isindicative of the width of the fingers. Pressure sensors may also beprovided on the fingers in order to measure the resilience and/orpressure and/or tension of tissue surrounding the fingers. The designaccording to FIGS. 14A and 14B is also usable for this purpose, possiblyfollowing removal of the cutting elements. Measurements can thus becarried out which are much more accurate than those carried out withconventional measurements, wherein use is made of a balloon or indirectmeasurement on the basis of a CT scan, echo and the like.

FIG. 15 shows a first design of the fourth aspect of this application.This first design relates to a prosthesis 1300 for the performance of anend-to-side (=ETS) anastomosis. This FIG. 15 is based on FIG. 10A fromWO 00/24339, on the understanding that the figure has been modified toshow the fourth aspect of the application. The modifications relating tothe fourth concept will be discussed below. Further details and alsovariants of the design shown, which were also present in the designaccording to WO 00/24339 and are also applicable to the fourth aspect ofthis application can be found in this WO 00/24339.

Memory metal, such as nitinol, has the favourable property that it canbe deformed from a first condition to a second condition, and can befixed in this second condition. By exceeding or understepping a specificthreshold temperature, the fixing can be undone, after which a reversedeformation from the second condition to the first condition takesplace. However, restrictions apply to this deformation and reversedeformation. If memory metal, such as nitinol, is deformed with anabrupt transition, as in the case of a sharp crease, permanentdeformations occur. As a result of these permanent deformations, thefinal condition remaining after reverse deformation differs from theoriginal first condition. It is even possible that little or nodeformation takes place. The memory then functions, so to speak, lesseffectively or not at all. To prevent this, it is customary to avoidsharp bends by using a concave shape, at the location of a sharp bend,so to speak in the axil thereof, which makes the bend much more gradual.In the case of ‘prostheses of the previously defined tubular type’, asharp bend is often required in the axil, resulting in a concave cavitywhich reduces the clamping force required for anchoring to the tissue atthe location of the axil. The fourth aspect of this application is alsointended to offer a solution to this problem.

The prosthesis 1300 comprises a tubular element 1301 formed from memorymaterial, in this case a nitinol alloy, with a distal flange 1320 and aproximal flange 1330. At 1312, a graft vessel 1310 is attached to thetubular element. This attachment may be carried out in the mannerdescribed in WO 00/24339, but can also be done in a different manner,such as through adhesion, and/or at a location other than at 1312.

The distal flange and proximal flange or both shown here in the radialposition, in which they extend in a radially outward direction inrelation to the tubular element.

The distal flange 1320 is formed by a plurality of distal flange feet1302, which are disposed in a distributed manner over the circumferenceof the tubular element 1301.

The distal flange feet are releasable from an extended positionindicated schematically with broken lines to tilt to the radial position(arrow E). In the radial position, the distal flange feet, together withthe proximal flange, around a passage formed in the receiving vessel,clamp the surrounding tissue 1311 of the wall of the receiving vessel.

The surrounding tissue 1311 of a receiving vessel in the case of an ETSanastomosis is usually quite thin. This is illustrated in FIG. 15 byshowing the distal flange and the proximal flange in the radial positionwith an intermediate space between them. It will be clear that, inreality, the distal flange and proximal flange 1320 and 1330 must lie inthe radial position against the tissue 1311 in order to clamp it.

By way of departure from the knowledge disclosed by WO 00/24339, thedistal flange feet are provided at the ends thereof which are attachedto the tubular element with a filling 1305. In the radial position, thisfilling results in an increased clamping force of the distal flange andproximal flange, in particular at the location of the filling 1305. As asecondary effect, the increased clamping force also results in animproved seal. According to a further design of the fourth aspect, thedistal flange feet 1320 are provided with a concave-curved part 1304which follows on from the ends of the distal flange feet attached to thetubular element. The filling 1305 is disposed here in the hollow side ofthe concave-curved part 1304 facing towards the proximal flange. Thedistal flange feet can optionally have a straight part 1306 whichconnects the concave-curved part 1304 to the free end of the distalflange feet.

As described in WO 00/24339, it is very readily possible in the case ofan ETS anastomosis to design the proximal flange 1330 as a fixed flangewhich is permanently in the radial position. According to the fourthaspect, a filling 1308 can be provided in this case also on the insideof the proximal flange, and the proximal flange can optionally beprovided with a concave-curved part 1307. However, it is also veryreadily possible according to the fourth aspect of this application todesign the proximal flange 1330 corresponding to the distal flange 1320with proximal flange feet 1303 which, corresponding to the distal flangefeet 1302, can tilt from an extended position to a radial position, andwhich, corresponding to the distal flange feet, are provided with afilling 1308 which may optionally be housed in the cavity of aconcave-curved part 1307, and which may optionally have a straight part1309.

It is noted that the principle of the filling, according to the fourthaspect of this application, is applicable to essentially all designs asdescribed and shown in WO 00/24339. For this reason, this WO 00/24339 isdeemed to be included in full in this application.

FIGS. 16A and 16B show a second design of the fourth aspect of thisapplication. This second design relates to a prosthesis 1400 forattaching a heart prosthesis to surrounding tissue, such as a valveannulus. This FIGS. 16A and 16B is based on FIG. 2 from WO 00/44311, onthe understanding that the figure has been modified to show the fourthaspect of the application. The modifications relating to the fourthconcept will be discussed below. Further details and also variants ofthe design shown in FIGS. 16A and 16B, which were also present in thedesign according to WO 00/44311 and are also applicable to the fourthaspect of this application, can be found in this WO 00/44311.

The prosthesis 1400 comprises a tubular element 1401 formed from memorymaterial, in this case a nitinol alloy, with a distal flange 1420 and aproximal flange 1430. According to the fourth aspect, a valve prosthesiswith a heart valve can be attached, if required, to the tubular element1401. This can be done in many different ways already known from WO00/44311.

The distal flange and proximal flange are both shown here in FIG. 16B inthe radial position, in which they extend in a radially outwarddirection in relation to the tubular element 1401. The distal flange4020 is formed by a plurality of distal flange feet 1402, which aredisposed in a distributed manner over the circumference of the tubularelement 1401 with intermediate spaces 1415 between them. The proximalflange 1430 is similarly formed by a plurality of proximal flange feet1403, which are disposed in a distributed manner over the circumferenceof the tubular element 1401 with intermediate spaces 1416 between them.The distal and proximal flange feet 1402, 1403 are releasable from theextended position shown in FIG. 16A to tilt to the radial position(Arrow E). In the radial position, the distal flange feet 1402, togetherwith the proximal flange feet 1403, clamp firmly on a valve annulus1411. By way of departure from the knowledge disclosed in WO 00/44311,the distal flange feet 1402 and proximal flange feet 1403 are providedat the ends thereof which are attached to the tubular element 1401 witha filling 1405 and 1408 respectively. In the radial position, thesefillings result in an increased clamping force of the distal flange andproximal flange on the annulus 1411, in particular at the location ofthe fillings 1405 and 1408. As a secondary effect, the increasedclamping force also results in an improved seal. According to a furtherdesign of the fourth aspect, the distal and proximal flange feet 1420and 1430 are provided with a concave-curved part 1404 and 1407respectively, which follows on from the ends of the distal and proximalflange feet attached to the tubular element 1401. The fillings 1405 and1408 are disposed here in the hollow side of the concave-curved part1404 and 4007 facing towards the proximal flange.

As described in WO 00/44311, it is very readily possible in the case ofa prosthesis of this type to design the proximal flange 1430 as a fixedflange which is permanently in the radial position. In this case also,according to the fourth aspect, a filling 1408 can also be provided onthe inside of the proximal flange.

It is noted that the principle of the filling, according to the fourthaspect of this application, is essentially applicable to all designs asdescribed and shown in WO 00/44311, in particular sections 1.1, 2.1,3.1, 4.1 and associated FIGS. 1-14. For this reason, the sections 1.1,2.1, 3.1, 4.1 and associated FIGS. 1-14 of this WO 00/44311 are deemedto be included in their entirety in this application.

FIGS. 17, 18 and 19 show a ring structure (1600) according to the sixthaspect of this application.

FIG. 17 shows the ring structure in an opened, flatly laid out view.Here, the ring shape can be obtained by attaching the left end and theright end of the illustration to one another and by forming thestructure flatly laid out in the illustration into a ring.

The ring structure has an axial direction represented by the axialcentre line 1605 and a radial direction R disposed across it (FIG. 18 ).The ring structure is constructed from a series of elongated loops 1610,the longitudinal direction of which extends in FIG. 17 in the axialdirection, and the lateral direction of which extends in the tangentialdirection T (circumferential direction) of the ring structure 1600.

Adjacent loops 1610 are connected roughly at the midpoint of the longsides of the loop in each case via a junction 1611 to the respectiveadjacent loop. The imaginary centre line 1612 which interconnects thesejunctions forms a ring and divides each loop globally into a first half1601 and a second half 1602.

The first half 1601 of each loop in each case forms a proximal flangefoot and the second half 1602 of each loop in each case forms a distalflange foot. These flange feet are shown in FIG. 17 in the so-calledextended condition, i.e. the condition in which they are orientedprimarily in an axial direction. As shown in FIG. 18 , in thenon-expanded condition with diameter X1, the free ends 1606 and 1607 ofthe flange feet point, in the extended position, in the axial direction,but the flange feet 1603 and 1604 do not have to run purely axially inthe extended position.

The proximal flange feet 1603 and the distal flange feet can bendoutwards from the extended condition to a radial position. In the radialposition, the free ends 1606 and 1607 of the flange feet point in theradial direction R. This outward bending occurs automatically, since theflange feet have been pre-tensioned for this purpose with a force(represented by curved arrows 1609 in FIG. 18 ) which is inclined tobend these flange feet to the radial position. This pre-tension may be afrozen temporary condition of a memory material. The ring structure maybe made from a memory metal, such as a nitinol alloy, for this purpose.The pre-tension may also be a normal resilience (e.g. if the ringstructure is made from a spring-steel type of material). In this lattercase, a mechanical obstacle, such as a sleeve or obstacle elementsaccording to the seventh aspect, will be used to hold the flange feetstretched.

FIG. 17 shows the ring structure in an expanded condition. The loops arespread in the lateral direction in such a way that they have an innerwidth which in this case corresponds to 2 x the thickness of the loop.It will thus be clear that by, as it were, closing the loops (making theinner width zero by pressing the longitudinal sides against oneanother), a circumferential reduction of 50% can be implemented.

FIG. 17 furthermore shows that each junction 1611 is provided with one(or more) radial bores 1614. By means of these radial bores, a stent,heart valve or other biological or otherwise prosthesis can be attachedin the ring structure, for example simply by means of a suture.

FIG. 18 shows that the ring structure can be extended from a compressedcondition with diameter X1, which may, for example, be 13.3 mm, to anexpanded condition with diameter X2, which may, for example, be 26.6 mm.FIG. 18 furthermore shows that, after the expanded condition has firstbeen reached, the flange feet 1603 and 1604 are bent to the radialposition in order to clamp annulus tissue 1608 or other tissue betweenthem. In order to improve the fixing near or on the annulus of themitral or tricuspid valve, the flange feet 1604 (lowermost in FIG. 18 )are provided with a bulge 1615. This bulge 1615 is located in the half1616 of the relevant flange foot 1604 which follows on from thejunction. This bulge 1615 is adapted to the natural anatomy of themitral or tricuspid annulus.

FIG. 18 furthermore shows by means of the arrow 1613 that the ringstructure, if it is in the compressed condition, is under a radialpre-tension, which allows the expansion to occur automatically followingrelease of the pre-tension. However, it is noted that it is alsoconversely possible for the ring structure to be under a radiallyinwardly directed pre-tension in the expanded condition. The ringstructure is then usable, inter alia, as a constriction ring or as asealing ring which draws the surrounding tissue inwards to provide aseal against a prosthesis implanted therein.

FIG. 19 shows, as an example, a use of the ring structure 1600 as afixing means for the fixing on the annulus of a mitral valve of a stent1618 with a heart valve 1617 of biological material, a so-called valvedstent, therein.

FIG. 20 shows a manipulator 1700 according to the seventh aspect. Thismanipulator is intended for a prosthesis with distal and proximal flangefeet, which are both to be brought into an extended axial condition inwhich they are under pre-tension which is inclined to bend these flangefeet to a radial position. The proximal and distal flange feet areprovided on a ring or tubular element 1720 (of which only a very smallpart is shown in FIGS. 21A and 21B). The manipulator according to theseventh aspect is able to hold these flange feet in the extendedposition and to release them so that they can bend to the radialposition.

The manipulator 1700 is constructed from a plurality of U-shapedobstacle elements 1710 which are attached via cords 1716 to an operatingelement 1715. Each obstacle element has a first leg 1711 and a secondleg 1712, the free ends 1713, 1714 of which point in the distaldirection. The first leg 1711 has a first length L2 and the second leg1712 has a fourth length L4.

In the extended condition, the proximal flange feet 1703 have a thirdlength L3. The distance between the free ends 1704 and 1705 of theproximal flange feet and the distal flange feet, in the extendedcondition of the flange feet, is L1. FIG. 21A shows that L2 is longerhere than L1 and that L3 is shorter than L4. By taking L4 as slightlyshorter than L3, the second leg 1712 can be prevented from touching aprosthesis mounted in the ring or tubular part 1720.

In FIGS. 21A and 21B, the flange feet 1702 and 1703 are shown in theextended condition. The proximal flange foot extends into the cavitybetween the first leg 1711 and the second leg 1712. The first leg 1711is longer than the second leg 1712. The first leg extends along theradial outside of the prosthesis 1701, so that it holds in place theflange feet 1702 and 1704, which, as a result of the pre-tensionaccording to the arrows 1725, are inclined to bend outwards. The shortleg 1712 thereby ensures that the long leg is not pushed aside. Theproximal flange foot 1703 may, under the influence of the pre-tension,brace itself between the short leg 1712 and the long leg. This bracingmay be sufficient to prevent the U-shaped obstacle elements 1712 fromprematurely coming loose from the flange feet. If the prosthesis is atits intended location and the flange feet can be released, themanipulator is drawn away in the proximal direction P by means of theoperating element 1715 which carries the obstacle elements 1710 alongwith it via the cords 1716. The flange feet then bend outwards, forexample to the curved shape as shown in FIG. 21B.

Given that the cords 1716 are flexible, the obstacle elements 1710 cansimply move along with the prosthesis if the latter is expanded orcompressed. The release of the flange feet can therefore be implementedindependently from the expansion condition of the prosthesis. Theobstacle elements 1710 and/or the cords 1716 may furthermore beinterconnected by means of further cords (not shown here) or otherwise,as long as the free mobility in the radial and axial direction of theobstacle elements is not thereby hindered.

FIGS. 22 and 23 show port assemblies according to the eighth aspect.

FIG. 22 shows a first port assembly 1800. The first port assembly 1800comprises a connector 1802 and a closing cap 1803. FIG. 22 furthermoreshows the lowermost part of a work channel 1801 which can be attached tothe connector.

The connector 1802 is provided with an inner screw thread 1804 and thecap is provided with an outer screw thread 1805, with which the cap canbe screwed firmly into the connector. Recesses 1840 are provided in thetop of the cap in order to grip hereon with a tool for rotating the cap.

The connector 1802 is furthermore provided with an outer screw thread1807. A work channel 1801 provided with a mating inner screw thread 1806can thus be attached to the connector.

The connector is provided on the second end 1828 with a crosswisesurface with 3 concentric annular slots 1808, 1809 and 1810 therein,which extend completely around the port passage 1830. The inner slot1810 and the outer slot 1808 are connected via a channel to a connectionstub 1812, and the middlemost slot 1809 is separated from the inner andouter slot and opens out into its own connection stub 1811. Theconnection stub 1812 can be connected to a source for tissue adhesive,whereas the connection stub 1811 can be connected to a suction source inorder to be able to generate a suction force in the slot 1809, or viceversa. The connector can thus be sucked firmly onto the wall 1829 oftissue and can be adhered firmly thereto by means of tissue adhesive andcan be effectively sealed thereon.

A work channel 1820, 1822 is connectable to the first connector end1838. The work channel has a stiff or stiffened channel part 1822 and aflexible channel part 1820. The flexible channel part 1820 is attachedby means of the part 1801 to the connector and by means of theattachment 1821 to the stiff channel part 1822. The flexible channelpart is shown here as a vascular prosthesis, but may equally consist ofother flexible materials, such as, for example, rubber, silicone orplastics and other artificial materials, but also other curved orotherwise, hardened metal or plastic parts, which are reciprocallyshiftable, twistable or rotatable. The stiff channel part is provided onits upper end with a closure 1824 which can close the work channel onthe one hand and, on the other hand, can allow instruments herein. Theclosure may, for example, be a vascular prosthesis or hose which caneasily be squeezed tight. The connections 1801, 1821, and 1823 are shownhere as recesses over which a piece of vascular prosthesis is placedover which in turn a ligature or adhesion or ring or band or the like isplaced, said last tying means not being shown here, but essentially anyform of mechanical connection can be used. The work channel 1822 isfurthermore provided with a connection 1825 and 1826. Gassing ordegassing, for example, can be carried out via the one connection. Fluidcan be fed in or out, for example, via the other connection. Theconnections 1825 and 1826 can also be used to guide instruments inside.

The connections 1825, 1826, 1811 and 1812 may, for example, be Luerconnections.

The flexible channel part 1820 makes it possible, in a manner ofspeaking, to bend the longitudinal centre line 1827 of the work channelwithout bending the stiff channel part. The length of the stiff channelpart will be more than 10× that of the flexible channel part.

FIGS. 24A and 24B show very schematically an assembly 1900, for examplefor using the method according to the ninth aspect. FIG. 24A shows a topview and FIG. 24B shows, as a detail, a cross-section view, viewed inthe tangential direction of the assembly.

This assembly comprises, on the one hand, a heart prosthesis, such as aheart valve prosthesis, the heart valve of which is shown veryschematically with 1906 (FIG. 24B). The heart valve prosthesis comprisesan annular or tubular edge part 1905, with uppermost flange feats 1902and lowermost flange feet 1904. Annulus tissue can be clamped betweenthese flange feet. This heart valve prosthesis may, in principle, be ofany type, such as, inter alia, those known from the prior art. WO00/44311 of the inventor, for example, can be cited as an example, whichdesignates various suitable heart valve prostheses with movablelowermost and/or uppermost flange (feet). Although not necessary, radialslots 1903 are provided in the uppermost flange (possibly also in thelowermost flange).

The assembly for use of the ninth aspect furthermore comprises a ringprosthesis according to the second aspect of this application. This ringprosthesis is not shown in its entirety in FIG. 24A, but two ringsections of around 120° are shown. The one ring section, the wire ofwhich is shown with unbroken lines, is in the expanded condition. Theother ring section, the wire of which is shown by a broken line, is inthe contracted condition. The ring prosthesis comprises a waved wire802, with wave peaks 804, wave troughs 803 and pins 801. The pins 802are shown here as attached to the wave troughs 803. However, the pinsmay also be attached to the wave peaks 804 or elsewhere between the wavetroughs 803 and wave peaks 804.

The pins 801 of the ring prosthesis project through the radial slots1903 and can move backwards and forwards through the slots in a radialdirection. The implantation and attachment of the valve prosthesis cantake place here prior to or simultaneously with the implantation of thering prosthesis. However, the ring prosthesis may be integrated inadvance with the valve prosthesis, and preferably with the upper flangethereof. This integration could comprise the attachment of the ringprosthesis to the proximal side or to the distal side of the upperflange, wherein, in the latter case, the pins of the ring prosthesisproject through the radially positioned slots of the upper flange. It isalso possible to design the upper flange as double-walled, as indicatedschematically by means of broken lines 1910 in FIG. 24B. The ringprosthesis is then located between the two walls and the pins of thering prosthesis project through radially positioned slots. It will beclear that a radial spring, which in each case pre-tensions a pin in aradially inward direction, can also very readily be inserted in thehollow space which is created in the case of a double-walled design. Ifthe ring prosthesis is pre-tensioned in order to draw the pins in aradially inward direction, i.e. is pre-tensioned to reduce in diameter,the ring prosthesis then ensures that the tissue, such as the valveannulus, which is located between the lowermost flange 1904 and theuppermost flange 1902, is drawn in a radially inward direction. Thetissue is thus drawn against the outside of the annular or tubular edgepart 1905. The sealing of the tissue on the ring prosthesis can thus beimproved and the bypass of blood outside along the valve prosthesis canbe prevented. It will be clear that a different type of ring prosthesiswith radially inwardly pre-tensioned pins is also possible. The ringprosthesis could, for example, comprise a fixed-diameter ring withsprings radially mounted thereon and projecting outwards or inwards,which, on the other end, will be the pins which are oriented in an axialdirection. It is also conceivable here to dispense with a separate ringand to attach the aforementioned springs directly to the outer flange orinner flange of the heart valve prosthesis. The assembly can thus bereplaced with a heart valve prosthesis with at least one flange, said atleast one flange being provided with radial slots, wherein pins, whichare axially oriented and driven (pushed and/or pulled) radially inwardsby means of a spring, project through the radial slots. Finally, it isnoted that, wherever a spring is mentioned in this paragraph, this mayalso be a radially oriented zigzag wire made from a memory metal, suchas nitinol, the pre-tension of which is released in the event of heatingto above a threshold temperature.

The various designs of the nine aspects of this application can also beformulated in the clauses below:

1. Medical instrument, comprising:

-   -   a first rod (1);    -   a second rod (2) which extends along the first rod (1);    -   a longitudinal centre line (3) defined by the direction in which        the first rod (1) and the second rod (2) extend; and    -   a manipulator;        wherein the manipulator comprises at least a plurality of        fingers (4; 94; 144), each with a first finger end (5) and a        second finger end (6); wherein the second finger ends (6) are        free ends (6);        wherein the first finger ends (5) of this aforementioned        plurality of fingers are supported on the second rod (2) in such        a way that the fingers (4; 94; 144) of this aforementioned        plurality of fingers, by moving the second rod (2) in relation        to the first rod (1), are operable to be displaced from a first        position to a second position; and        wherein the distance from the free ends (6) of the fingers (4)        to the longitudinal centre line (3) in the first position is        different compared with the second position.        2. Medical instrument according to one of the preceding clauses,        wherein the first rod (1) and the second rod (2) are movable in        relation to one another in the longitudinal direction of the        longitudinal centre line (3) for the aforementioned operation of        the fingers (4; 94; 144).        3. Medical instrument according to one of the preceding clauses,        wherein the first rod (1) and the second rod (2) are rotatable        in relation to one another around the longitudinal centre line        (3) for the aforementioned operation of the fingers (4; 94;        144).        4. Medical instrument according to one of the preceding clauses,        wherein, in the second position or the first position, the        distance from the free ends (6) of the fingers (4) to the second        rod (2) is at most 90%, in particular at most 80%, such as at        most 75% or at most 70%, of the distance from the free ends (6)        of the fingers (4; 94; 144) to the second rod (2) in the other        of these two positions.        5. Medical instrument according to one of the preceding clauses,        wherein the plurality of fingers (4; 94; 144) is disposed in a        distributed manner over the circumference of the longitudinal        centre line (3).        6. Medical instrument according to one of the preceding clauses,        wherein the free, second finger ends (6) are provided with a        hook (60) with a hook opening (61) which opens in the direction        of the first finger ends (5).        7. Medical instrument according to one of the preceding clauses,        further comprising a tensioning system (62) acting on the        fingers (4; 94; 144) in order to pre-tension the latter for        displacement from the first position to the second position.        8. Medical instrument according to clause 7, wherein the        tensioning system comprises a resilient element (62) provided in        the circumferential direction of the instrument along the        fingers.        9. Medical instrument according to one of the preceding clauses,        wherein the distance from the free ends (6) of the fingers (4)        to the longitudinal centre line (3) is greater in the first        position than in the second position.        10. Medical instrument according to one of the preceding clauses        1-9, wherein the fingers (4; 94; 144) are movable from the first        position to the second position and from the second position to        a third position, wherein the distance from the free ends (6) of        the fingers (4) to the longitudinal centre line (3) in the first        position is greater than in the second position, and wherein the        distance from the free ends (6) of the fingers (4) to the        longitudinal centre line (3) in the third position is less than        in the second position.        11. Medical instrument according to one of the preceding        clauses, wherein the fingers (4) are attached at the first        finger ends (5) in a pivotable manner via a pivot attachment        (32, 33) to the second rod (2).        12. Medical instrument according to clause 11, wherein the        distance from the pivot attachment (32, 33) of the first finger        ends (5) to the longitudinal centre line (3) is unchanging.        13. Medical instrument according to one of the preceding        clauses, wherein the pivot attachment comprises a hinge (32,        33).        14. Medical instrument according to clause 13, wherein the hinge        comprises a convex part (32) and a corresponding concave        receptacle (33) for the convex part (32).        15. Medical instrument according to clause 14, wherein the        fingers (4; 94; 144) are in each case provided with an        aforementioned concave receptacle (33).        16. Medical instrument according to one of the preceding        clauses, wherein each finger (4; 94; 144) further comprises an        inner longitudinal side (7) facing towards the longitudinal        centre line (3), and an outer longitudinal side (8) facing away        from the longitudinal centre line (3);        wherein the medical instrument further comprises:    -   an inner guide (51; 36) provided between the longitudinal centre        line (3) and the inner longitudinal side (7) of the fingers (4);        and    -   an outer guide (52; 37), wherein the fingers (4) are provided        between the outer guide (52; 37) and the longitudinal centre        line (3);        wherein the first rod (1) carries the inner guide (51; 36) and        the outer guide (52; 37);        wherein each finger (4; 94; 144) has a first curved zone (9)        which defines a first finger part (10) which extends from the        first finger end (5) to the first curved zone (9) and a second        finger part (11) which extends from the first curved zone (9) to        the free end (6) of the finger (4; 94; 144);        wherein, viewed from the first finger ends (5) to the second        finger ends (6), the fingers (4; 94; 144) in the first curved        zone (9) bend away from the longitudinal centre line (3);        wherein, in the second position, the outer guide (52) grips on        the outer longitudinal side (8) of the second finger part (11)        of the fingers (4; 94; 144).        17. Medical instrument according to clause 16, wherein, in the        first position, the inner guide (51; 36) grips on the inner        longitudinal side (7) of the first finger part (10) of the        fingers (4; 94; 144).        18. Medical instrument according to one of clauses 16-17,        wherein, in the second position, the inner longitudinal side (7)        of the second finger part (11) of the fingers (4; 94; 144) lies        free from the inner guide (51; 36).        19. Medical instrument according to one of clauses 16-18,        wherein, in the first position, the outer longitudinal side (8)        of the first finger part (10) of the fingers (4; 94; 144) lies        free from the outer guide (52; 37).        20. Medical instrument according to one of clauses 16-19,        wherein, in the first position, the outer guide (52; 37) grips        on the outer longitudinal side (8) of the first finger part (10)        of the fingers (4; 94; 144).        21. Medical instrument according to clause 20, wherein, in the        first position, the outer longitudinal side (8) of the second        finger part (11) of the fingers (4; 94; 144) lies free from the        outer guide (52; 37).        22. Medical instrument according to one of clauses 16-21,        wherein, in the second position, the inner guide (51; 36) grips        on the inner longitudinal side (7) of the first finger part (10)        and/or the second finger part (11) of the fingers (4; 94; 144).        23. Medical instrument according to clause 22, wherein, in the        second position, the inner longitudinal side (7) of the first        finger part (10) of the fingers (4; 94; 144) lies free from the        inner guide (51; 36).        24. Medical instrument according to one of clauses 16-23,        wherein the fingers (4; 94; 144), in the aforementioned first        curved zone (9), show a curve of at least 30°, in particular a        curve of at least 45°, such as a curve of 50° or more.        25. Medical instrument according to one of clauses 16-24,        wherein the fingers (4; 94; 144) show a kinked shape in the        first curved zone (9), at least on the inner longitudinal side        (7) of the fingers (4; 94; 144).        26. Medical instrument according to one of clauses 16-25,        wherein the inner guide (51; 36) and the outer guide (13; 37)        are immovable in relation to one another.        27. Medical instrument according to one of clauses 16-26,        wherein the inner guide (51; 36) is designed, in order to guide        the free ends (6) of the fingers (4) in a radially outward        direction and in relation to the longitudinal centre line (3),        when the aforementioned movement of the first rod (1) in        relation to the second rod (2) takes place, in such a way that        the fingers (4; 94; 144) move to the first position.        28. Medical instrument according to one of clauses 16-27,        wherein the outer guide (13) is formed by a side of an annular        edge (37) provided on the first rod (1) and facing towards the        free ends (6) of the fingers (4).        29. Medical instrument according to one of clauses 16-28,        preferably in combination with at least clause 27, wherein, in        the first position, a slit is located between the fingers (4;        94; 144) and the inner guide (51; 36) with a radial size such        that, with the aforementioned movement of the first rod (1) in        relation to the second rod (2) in such a way that the fingers        (4; 94; 144) move in the direction of the first position, the        free ends (6) of the fingers (4; 94; 144) approach the        prosthesis (40; 80) from the inside thereof.        30. Medical instrument according to one of clauses 16-29,        wherein the outer guide (13; 37) extends around the longitudinal        centre line (3) and, preferably, has a diameter smaller than the        inner diameter of the prosthesis (40; 80).        31. Medical instrument according to one of the preceding        clauses,        wherein the second rod (2) has a first conical guide surface        (101);        wherein the fingers (4; 94; 144) of the aforementioned plurality        of fingers, at the first finger ends (5), have a guide part        (102) which can be displaced along and in contact with the first        conical guide surface (101) in order to displace the fingers (4;        94; 144) from this first position to this second position,        wherein the distance from the guide parts (102) to the        longitudinal centre line in the first position is different        compared with the second position.        32. Medical instrument according to clause 31, wherein the guide        part (102) of an aforementioned finger (4; 94; 144) and the        remainder of an aforementioned finger (4; 94; 144) are rigid in        relation to one another.        33. Medical instrument according to one of clauses 31-32,        wherein the distance from the fingers (4; 94; 144) to the        longitudinal centre line (3) in the second position is greater        than in the first position.        34. Medical instrument according to one of clauses 31-33,        wherein the fingers (4; 94; 144) can be slid back from the        second position, along and in contact with the guide surface, in        the direction of the first position.        35. Medical instrument according to one of the preceding clauses        31-34, wherein the fingers (4; 94; 144) extend parallel to the        longitudinal centre line (3).        36. Medical instrument according to one of the preceding clauses        31-35, wherein the instrument further comprises:        a second conical guide surface (103);        a second plurality of fingers (94), each with a first finger end        (5) and a second finger end (6);        wherein the second finger ends (6) of the second plurality of        fingers (94) are free ends;        wherein the fingers (94) of the second plurality of fingers, at        the first finger ends (5), have a guide part (102) which is        shiftable along and in contact with the second conical guide        surface (103) from a first position to a second position, in        which the distance from the guide parts (102) of the second        plurality of fingers (94) to the longitudinal centre line is        different compared with the first position;        wherein the first and second conical guide surfaces (101, 103)        are mirrored in relation to one another, such as facing towards        one another; and        wherein the free ends (6) of the first plurality of fingers (4)        are pointed towards the free ends (6) of the second plurality of        fingers (94) and the free ends (6) of the second plurality of        fingers (94) are pointed towards the free ends (6) of the first        plurality of fingers (4).        37. Medical instrument according to clause 36, wherein the first        rod (2) is connected to the first (4) and/or second (94)        plurality of fingers for the operation thereof.        38. Medical instrument according to one of clauses 36-37,        further comprising a third rod (91) which extends along the        second rod (2) and is connected to the second plurality of        fingers (94) for the operation thereof.        39. Medical instrument according to one of the preceding        clauses,        wherein the first rod (1) is provided with a slotted element        (34) with slots (35) which extend in the longitudinal direction        of the first rod (1);        wherein the fingers (4; 94; 144) of an aforementioned plurality        of fingers extend in each case through an aforementioned slot        (35);        wherein, in the one of the aforementioned first and second        positions, the free ends (6) of these fingers (4; 94; 144)        project outwards from the slots; and wherein, in the other of        the aforementioned first and second positions, the free ends (6)        of these fingers (4; 94; 144) are sunk entirely into the slots        (35).        40. Medical instrument according to clause 39, wherein the slots        (35) have slot bases (36) which are designed as guide surfaces        to guide the free finger ends (6) in a radial direction in the        event of displacement of the second rod (2) in relation to the        first rod (1).        41. Medical instrument according to one of clauses 39-40,        wherein, in the one of the aforementioned first and second        positions, in which the free finger ends (6) contact the outside        of a hollow prosthesis provided on the instrument, a slit is        provided between the fingers (4; 94; 144) and the slot bases        (36) with a radial size such that, in the event of movement of        the fingers (4; 94; 144) from the other of the aforementioned        first or second positions in the direction of the one of the        aforementioned first or second positions, the free finger ends        (6) approach the hollow prosthesis provided on the instrument        from the inside.        42. Medical instrument according to one of the preceding        clauses, wherein the instrument further comprises a stop (39),        such as a support ring, which, in the case of a prosthesis        provided on the instrument, is located proximally from the        prosthesis and is designed to prevent displacement of the        prosthesis in the proximal direction along the instrument.        43. Medical instrument according to clause 42, wherein the stop        is a support ring (39), which is attached to the first rod (1)        by means of a number, such as 2 or 3, of carrier arms (46)        disposed in a distributed manner over the circumference of the        first rod (1).        44. Medical instrument according to one of the preceding        clauses, wherein the instrument comprises, in use, a proximal        end pointed away from the patient and, in use, a distal end        pointed towards the patient, and wherein the plurality of        fingers (4; 94; 144) is provided at the distal end.        45. Medical instrument according to clause 44, wherein the        plurality of fingers comprises a first plurality of fingers (4),        the first finger ends (5) of which face towards the distal end        of the instrument and the free, second finger ends (6) of which        face towards the proximal end of the instrument; and wherein the        distance from the free ends (6) of the fingers (4) of the first        plurality of fingers (4) to the second rod (2) in the first        position is greater than in the second position.        46. Medical instrument according to clause 45, preferably in        combination with the following clause 67 or 68, wherein, in the        second position, the largest diameter defined by the first        plurality of fingers (4) is smaller than the inner diameter of        the prosthesis, in particular smaller than the inner diameter        which the prosthesis has after it has been detached from the        instrument.        47. Medical instrument according to one of clauses 45-46,        wherein the second rod (2) is displaceable in a distal direction        in relation to the first rod (1) for the aforementioned        operation of the fingers (4) of the first plurality of fingers.        48. Medical instrument according to one of clauses 45-47,        wherein the fingers (4) of the first plurality of fingers,        viewed from the first finger end (5) to the free, second finger        end (6), are kinked in a second curved zone (70) in a radially        inward direction, wherein this second curved zone is, in        particular, such that the part of the fingers (4) of the first        plurality of fingers, which is located on the side of the second        curved zone facing towards the second finger end (6), can extend        parallel to the longitudinal direction of the instrument,        whereas, viewed from the first finger ends (5) of the first        plurality of fingers (4) in the direction of the second curved        zone (70), the part of the fingers of the first plurality of        fingers which is located on the side of the second curved zone        facing towards the first finger end (5) protrudes in a radially        outward direction.        49. Medical instrument according to one of clauses 45-48,        wherein the free, second finger ends (6) of the first plurality        of fingers (4) are provided with a hook with a hook opening        which opens in the direction of the first finger ends.        50. Medical instrument according to one of clauses 44-49,        wherein the plurality of fingers comprises a second plurality of        fingers (94), the first finger ends (5) of which face towards        the proximal end of the instrument and the second finger ends        (6) of which face towards the distal end of the instrument, and        wherein the instrument may further comprise a third rod (91),        which extends along the first rod (1).        51. Medical instrument according to clause 50, wherein the        distance from the free ends (6) of the fingers (94) of the        second plurality of fingers to the longitudinal centre line (3)        in the first position is greater than in the second position.        52. Medical instrument according to clause 50 or 51, preferably        in combination at least clause 67 or 68, wherein, in the second        position, the largest diameter defined by the second plurality        of fingers (94) is smaller than the inner diameter of the        prosthesis, in particular smaller than the inner diameter which        the prosthesis has after it has been detached from the        instrument.        53. Medical instrument according to one of clauses 50-52,        wherein the third rod (91) is displaceable in relation to the        first rod (1) in the longitudinal direction of the centre line        (3) for the aforementioned operation of the fingers (94) of the        second plurality of fingers.        54. Medical instrument according to one of clauses 50-53,        wherein the fingers (94) of the second plurality of fingers,        viewed from the first finger end (5) to the free, second finger        end (6), are kinked in a second curved zone (70) in a radially        inward direction, wherein this second curved zone (70) is, in        particular, such that the part of the fingers (94) of the second        plurality of fingers, which is located on the side of the second        curved zone (70) facing towards the second finger end (6), can        extend parallel to the longitudinal direction of the instrument,        whereas, viewed from the first finger ends (5) of the second        plurality of fingers (94) in the direction of the second curved        zone (70), the part of the fingers (94) of the second plurality        of fingers which is located on the side of the second curved        zone (70) facing towards the first finger end (5) protrudes in a        radially outward direction.        55. Medical instrument according to one of clauses 50-54,        wherein the free, second finger ends (6) of the second plurality        of fingers (94) are provided with a hook (60) with a hook        opening (61) which opens in the direction of the first finger        ends (5) thereof.        56. Medical instrument according to one of clauses 44-45,        wherein the plurality of fingers comprises a third plurality of        fingers (144), the first finger ends (5) of which face towards        the proximal end of the instrument and the free, second finger        ends (6) of which face towards the distal end of the instrument;        and wherein the distance from the free ends (6) of the fingers        (144) of the third plurality of fingers to the longitudinal        centre line (3) in the first position is greater than in the        second position.        57. Medical instrument according to clause 56, preferably in        combination with the following clause 67 or 68, wherein, in the        second position, the largest diameter defined by the third        plurality of fingers (144) is smaller than the inner diameter of        the prosthesis, in particular smaller than the inner diameter        which the prosthesis has after it has been detached from the        instrument.        58. Medical instrument according to one of clauses 56-57,        wherein the second rod (2) is displaceable in relation to the        first rod (1) in the longitudinal direction of the centre line        (3) for the aforementioned operation of the fingers (144) of the        third plurality of fingers.        59. Medical instrument according to one of clauses 56-58,        wherein the fingers (144) of the third plurality of fingers,        viewed from the first finger end (5) to the free, second finger        end (6), are kinked in a first curved zone (9) in a radially        outward direction.        60. Medical instrument according to one of clauses 56-59,        wherein the free, second finger ends (6) of the third plurality        of fingers (144) are provided with a hook (60) with a hook        opening (61) which opens in the direction of the first finger        ends (5).        61. Medical instrument according to one of clauses 56-59,        wherein the fingers (144) of the third plurality of fingers,        viewed from the first finger end (5) to the free, second finger        end (6), are kinked in a second curved zone (70) in a radially        inward direction, and wherein this second curved zone (70) is,        in particular, such that the part of the fingers (144) of the        third plurality of fingers, which is located on the side of the        second curved zone (70) facing away from the first finger end        (5), can extend parallel to the longitudinal direction of the        instrument, whereas, viewed from the first finger ends (5) of        the third plurality of fingers (144) in the direction of the        second curved zone (70), the part of the fingers (144) of the        third plurality of fingers which is located on the side facing        towards the first finger ends (5) adjacent to the second curved        zone (70) protrudes in a radially outward direction.        62. Medical instrument according to one of the preceding        clauses, wherein the instrument is sterile.        63. Medical instrument according to one of the preceding        clauses, wherein the instrument is made from one or more        medically acceptable materials.        64. Medical instrument according to one of the preceding        clauses, wherein the first rod (1) has a carrier part (28) to        carry a prosthesis (40, 80, 90, 96, 800), and wherein the        fingers (4; 94; 144) of the at least one plurality of fingers        are movable in relation to the carrier part (28).        65. Medical instrument according to one of the preceding        clauses, wherein the instrument is intended for the implantation        of a prosthesis (40, 80, 90, 96, 800).        66. Medical instrument according to one of the preceding        clauses, further comprising a prosthesis (40, 80, 90, 96, 800),        wherein the free ends (6) of the fingers (4), in the one of the        aforementioned first and second positions, grip on the        prosthesis and, in the other of the aforementioned first and        second positions, preferably lie free from the prosthesis.        67. Medical instrument according to one of clauses 64-66,        wherein the prosthesis (40, 80, 90, 96) has a tubular element.        68. Medical instrument according to one of clauses 64-65,        wherein the prosthesis (40, 80, 90, 96) is a ‘prosthesis of the        type with a tubular element’ (42) with a distal (43) and        proximal (41) flange which extend along the circumference of the        tubular element, wherein the distal and/or proximal flange has        flange feet (44) which are bendable from an extended position        extending in an axial direction to a radial position extending        in a radial direction.        69. Medical instrument according to one of clauses 67 of 68,        wherein the carrier part (28) is designed to grip on the inside        of the tubular element (198) or organ (96).        70. Medical instrument according to one of clauses 64-69,        wherein biological tissue is located between the prosthesis (40,        80, 90, 96) and the instrument.        71. Medical instrument according to one of clauses 64-70,        wherein the prosthesis (40, 80, 90, 96, 800) is a heart        prosthesis, such as a heart valve prosthesis or ring prosthesis.        72. Medical instrument, wherein the prosthesis is one from the        group of:    -   a ring prosthesis (800) according to one of clauses 75-100;        and/or    -   a stent (90, 96) according to one of the following clauses        101-111; and/or    -   a stented valve prosthesis; and/or    -   a ‘prosthesis of the type with a tubular element’.        73. Medical instrument according to one of the preceding        clauses, wherein the first rod and/or second rod and/or third        rod are designed as flexible, such as bendable or kinkable, over        at least a part of the length thereof, in such a way that the        longitudinal centre line of the respective rod(s) is flexible,        such as bendable or kinkable.        74. Medical instrument according to clause 73,        wherein the first rod and/or second rod and/or third rod, over        at least a part of the length thereof, are designed from        superelastic material, such as nitinol designed in superelastic        form; and/or        wherein the first rod and/or second rod and/or third rod are        designed, over at least a part of the length thereof, as a wire,        such as steel wire.        75. Ring prosthesis (800) for the constriction of the        through-flow passage of a heart valve, wherein the ring        prosthesis (800) comprises:    -   a first ring (802); and    -   anchoring elements (801) to attach the first ring (802) to        tissue surrounding the through-flow passage to be constricted,        wherein each anchoring element (801) is attached to the first        ring (802);        wherein the first ring is formed from a wire (802) which, viewed        in the circumferential direction of the first ring, extends        along a waved pattern in such a way that the diameter of the        ring prosthesis (800) is constrictable from a first condition to        a second condition, wherein the wave lengths (L) of the waves of        the waved pattern in the aforementioned first condition are        greater than in the aforementioned second condition.        76. Ring prosthesis (800) according to clause 75, wherein the        waved wire is in the first position and the ring, in this first        position, is under a pre-tension, as a result of which the ring        is inclined to constrict to the second position.        77. Ring prosthesis (800) according to clause 75 or 76, wherein        the anchoring elements comprise pins (801).        78. Ring prosthesis (800) according to clause 77, wherein the        pins (801) extend in the axial direction of the first ring        (802).        79. Ring prosthesis (800) according to one of the preceding        clauses 77-78, wherein at least a part of the pins (801) is        pre-tensioned in order to displace the free ends, once the        pre-tension has been released, in relation to the ends of the        pins attached to the ring prosthesis.        80. Ring prosthesis (800) according to clause 79, wherein the        pins, or at least a part thereof, are pre-tensioned in order,        following release with the free ends, to    -   to be displaced in a radially inward direction; and/or    -   to be displaced in a radially outward direction; and/or    -   to be displaced in a tangential direction; and/or    -   to be displaced in pairs towards one another.        81. Ring prosthesis (800) according to one of the preceding        clauses 75-80, wherein the anchoring elements (801) are disposed        in a distributed manner, such as evenly distributed, over the        circumference of the first ring (802).        82. Ring prosthesis (800) according to one of the preceding        clauses 75-81, further comprising a plurality of segments (806)        disposed in a distributed manner over the circumference of the        first ring (802), wherein each segment (806) is attached to the        first ring (802).        83. Ring prosthesis (800) according to clause 82, wherein        segments adjacent in the circumferential direction may, in the        first condition, lie at a distance from one another leaving an        intermediate space free, and, in the second position, lying        against one another, may form an essentially closed second ring        which prevents further constriction.        84. Ring prosthesis (800) according to one of the preceding        clauses 75-83, wherein the amplitude of the waved pattern        extends in the radial direction of the ring.        85. Ring prosthesis (800) according to clause 84, wherein the        amplitude of the waved pattern extends at an angle of 30° to 90°        in relation to the axial direction (805) of the first ring        (802).        86. Ring prosthesis (800) according to one of clauses 75-85,        wherein the position of the amplitude of the waved pattern in        relation to the axial direction of the first ring, viewed along        the circumference of the first ring, varies.        87. Ring prosthesis (800) according to one of the preceding        clauses 75-86, wherein the ring prosthesis (800) comprises at        most one aforementioned anchoring element (801) for each wave        cycle of the waved pattern.        88. Ring prosthesis (800) according to one of the preceding        clauses 75-87, wherein the anchoring elements (801) are attached        to the first ring (802) in each case in the same part of the        wave cycle of the waved pattern.        89. Ring prosthesis (800) according to clause 87 or 88, wherein        the anchoring elements (801) are attached to the inward-facing        troughs (803) of the waved pattern, in particular at the        midpoint of these troughs.        90. Ring prosthesis (800) according to clause 87 or 88, wherein        the anchoring elements (801) are attached to the outward-facing        peaks (804) of the waved pattern, in particular at the midpoint        of these peaks.        91. Ring prosthesis (801) according to one of the preceding        clauses 75-90, wherein the waved pattern is a sinusoidal        pattern.        92. Ring prosthesis (801) according to one of the preceding        clauses 75-91, wherein the waved pattern comprises 8, 9, 10, 11,        12, 13, 14 or 15 wave cycles, wherein the first ring (802) has a        diameter in the 15 mm to 55 mm range.        93. Ring prosthesis (801) according to one of the preceding        clauses 75-92, wherein, viewed in the direction of the wave        height (H), the distance between the peaks (804) and troughs        (803) of the waves lies in the 0.5 mm to 20 mm range, such as in        the 0.5 to 3 mm range.        94. Ring prosthesis (800) according to one of the preceding        clauses 75-93, wherein the anchoring elements comprise clamping        mouths with a first jaw part (808) and a second jaw part (809)        which is movable in relation to the first jaw part in order to        clamp tissue between the jaw parts.        95. Ring prosthesis (800) according to clause 94, wherein the        clamping mouths are brought from a closed condition against        spring action to an open condition, and can be returned from the        opened condition to the closed condition under the influence of        said spring action.        96. Ring prosthesis (800) according to clause 95, wherein the        clamping mouths comprise a memory material which provides the        aforementioned spring action, and wherein the clamping mouths        are fixed in the opened condition by means of a temperature        treatment in order to be able to return to the closed position        if a threshold temperature is exceeded or understepped.        97. Ring prosthesis (800) according to one of clauses 94-96,        wherein the clamping mouths are provided on the outer        circumference of the ring prosthesis and are pointed with the        mouth opening in a radially outward direction.        98. Ring prosthesis according to one of clauses 94-97, wherein        the clamping mouths comprise one or more teeth which are        attached, in particular, to a jaw part and point towards the        opposite jaw part.        99. Ring prosthesis (800) according to one of clauses 75-98,        wherein an imaginary line, which forms the midpoint between the        wave troughs and wave peaks, defines a basic shape of the ring        prosthesis, and wherein this basic shape, viewed in the axial        direction of the ring prosthesis, is bean-shaped or        kidney-shaped.        100. Ring prosthesis (800) according to one of clauses 75-99,        wherein an imaginary line, which forms the midpoint between the        wave troughs and wave peaks, defines a basic shape of the ring        prosthesis, and wherein this basic shape is a 3-dimensional        shape, such as a sinusoidal shape.        101. Stent (96), comprising    -   a tubular element (198) which is expandable in a radial        direction from a compressed condition to an expanded condition,        and which has a proximal and distal end;    -   a proximal flange (83) of proximal flange feet provided around        the tubular element (196); and    -   a distal flange (82) of distal flange feet provided around the        tubular element (196);        wherein the distal (82) and proximal (83) flange feet are        attached with a fixed end to the tubular element (196) and have        another end which is free;        wherein the distal and proximal flange feet have a radial        position, in which the free ends of the flange feet point in a        radial direction for anchoring with surrounding tissue;        wherein the distal flange feet (82) are pivotable from an        extended position, in which the distal flange feet (82) lie in        the longitudinal direction of the tubular element (196), to a        radial position extending in a radial direction; and        wherein the distal flange feet (82) are provided distally from        the proximal flange feet (83).        102. Stent (96) according to clause 101, wherein the proximal        flange feet (83) are pivotable from an extended position, in        which the proximal flange feet (83) lie in the longitudinal        direction of the tubular element (198), to a radial position        extending in a radial direction.        103. Stent (96) according to one of clauses 101-102,        wherein the fixed ends of the distal flange feet (82) are        located at a distance from the distal end of the tubular element        (196) which is greater than 2× the length of the distal flange        feet (82); and        wherein the fixed ends of the proximal flange feet (83) are        located at a distance from the proximal end of the tubular        element (196) which is greater than 2× the length of the        proximal flange feet (83).        104. Stent (96) according to one of clauses 101-103, further        comprising a heart valve provided in the tubular element (196).        105. Stent (96) according to clause 104, wherein the heart valve        is a natural donor valve, such as from an animal or human.        106. Stent (96) according to clause 105, wherein the donor valve        is a biological valve chosen from the group of:    -   porcine valves; and/or    -   bovine valves; and/or    -   equine valves; and/or    -   human valves; and/or    -   kangaroo valves.        107. Stent (96) according to one of clauses 101-106, wherein the        separate flanges, or parts thereof, or the separate flange feet        of the separate flanges have an unequal shape and/or length        and/or width in relation to one another, and/or angle in        relation to the longitudinal axis, and/or fillings.        108. Stent (96) according to one of clauses 101-107, wherein the        fillings of the separate flanges, or the separate flange feet of        the separate flanges, have an unequal shape and/or length and/or        width in relation to one another, and/or angle in relation to        the longitudinal axis, and/or consistency and/or material        properties.        109. Stent (96) according to one of clauses 101-108, wherein the        fillings of the separate flange feet extend beyond the        circumference of a flange foot, and/or in a lateral and/or        radial direction therefrom.        110. Stent (96) according to one of clauses 101-109, wherein the        fillings of the separate flange feet are interconnected in such        a way that a continuity arises between all or a number of        fillings of the flange feet of one or both flanges.        111. Stent according to one of clauses 101-106, further        comprising a ring structure according to one of clauses 136-162,        which provides the proximal and distal flange feet.        112. Prosthesis for attachment in a passage surrounded by        tissue,        wherein the prosthesis comprises a tubular element formed from        memory material with a proximal and distal flange which extend        around the tubular element;        wherein the distal and proximal flange have a radial position,        in which they project from the tubular element in a radially        outward direction in order to clamp tissue surrounding the        passage between the distal and proximal flange;        wherein the distal flange consists of distal flange feet, which        are bendable from the radial position, against a pre-tension        created by the memory material, to an extended position, in        which the distal flange feet extend in the longitudinal        direction of the tubular element and which are fixable in this        extended position, in order to return to the radial position        under the influence of the pre-tension once the fixing has been        undone;        wherein the distal flange feet, at the ends attached to the        tubular element, are provided on the side facing the proximal        flange with a filling which is designed, in the radial position        of the distal and proximal flange, to increase the clamping        force with which the distal and proximal flange clamp the tissue        in situ.        113. Prosthesis according to clause 112, wherein the distal        flange feet have a concave-curved part which follows on from the        ends of the distal flange feet attached to the tubular element,        wherein the hollow side of the concave-curved part faces towards        the proximal flange, and wherein the filling is provided in the        hollow side of the concave-curved part.        114. Prosthesis according to clause 113, wherein the filling        projects from the concave-curved part in the direction of the        opposite flange feet.        115. Prosthesis according to clause 114, wherein the filling is        compressible, in such a way that, if the flange feet are in the        radial position, the part of the filling projecting from the        cavity can be compressed.        116. Prosthesis according to one of clauses 112-115, wherein the        concave-curved part of the distal flange feet, on the side        thereof facing towards the free ends of the distal flange feet,        viewed in the radial direction and radial position, changes to a        straight part.        117. Prosthesis according to one of clauses 112-116, wherein the        proximal flange consists of proximal flange feet, which are        bendable from the radial position, against a pre-tension created        by the memory material, to an extended position, in which the        proximal flange feet extend in the longitudinal direction of the        tubular element and which are fixable in this extended position,        in order to return to the radial position under the influence of        the pre-tension once the fixing has been undone;        wherein the proximal flange feet, at the ends attached to the        tubular element, are provided on the side facing the distal        flange with a filling which is designed, in the radial position        of the distal and proximal flange, to increase the clamping        force with which the distal and proximal flange clamp the tissue        in situ.        118. Prosthesis according to clause 117, wherein the proximal        flange feet have a concave-curved part which follows on from the        ends of the proximal flange feet attached to the tubular        element, wherein the hollow side of the concave-curved part        faces towards the distal flange, and wherein the filling is        provided in the hollow side of the concave-curved part.        119. Prosthesis according to one of clauses 117-118, wherein the        concave-curved part of the proximal flange feet, on the side        thereof facing towards the free ends of the proximal flange        feet, viewed in the radial direction and radial position,        changes to a straight part.        120. Prosthesis according to one of clauses 112-119, wherein the        filling is made from a material other than the material from        which the tubular element, the distal flange and the proximal        flange are made.        121. Prosthesis according to one of clauses 112-120, wherein the        filling is made from a foam-like material and/or a textile        and/or a plastic.        122. Prosthesis according to one of clauses 112-121, wherein the        memory material is a memory metal.        123. Prosthesis according to clause 122, wherein the memory        metal is a nitinol alloy.        124. Prosthesis according to one of clauses 112-123, wherein the        separate flanges, or parts thereof, or the separate flange feet        of the separate flanges have an unequal shape and/or length, or        width in relation to one another, and/or angle in relation to        the longitudinal axis, and/or fillings.        125. Prosthesis according to clauses 112-124, wherein the        fillings of the separate flanges, or the separate flange feet of        the separate flanges, may have an unequal shape and/or length        and/or width in relation to one another, and/or angle in        relation to the longitudinal axis, and/or consistency and/or        material properties.        126. Prosthesis according to clause 112-125, wherein the        fillings of the separate flange feet extend beyond the        circumference of a flange foot, and/or in a lateral and/or        radial direction therefrom.        127. Prosthesis according to clause 112-126, wherein the        fillings of the separate flange feet are interconnected in such        a way that a continuity arises between all or a number of        fillings of the flange feet of one or both flanges.        128. Applicator (1500) for the implantation of a hollow        prosthesis with an open distal end and an open proximal end,        comprising:    -   a tube (1501) with an inner screw thread over at least a part of        the length thereof;    -   a pin (1502) extending through the tube (1501) with, over at        least a part of the length thereof, an outer screw thread (1507)        which mates with the aforementioned inner screw thread;        wherein the tube (1501) carries a sheathing (1505) on the distal        end thereof;        wherein the pin (1502) is equipped, on the distal end thereof,        with a carrier (1504) for a prosthesis (802), said carrier        (1504), on the one hand, being rotatable in relation to the pin        (1502) around the longitudinal centre line of the pin and, on        the other hand, being shiftable from a position pushed out from        the sheathing (1505) in the proximal direction in relation to        the sheathing (1505) to a position entirely or partially        retracted into the sheathing, by rotating the tube (1501) in        relation to the pin; and wherein the applicator further        comprises an axial guide (1507) which is designed, on the one        hand, to prevent rotation of the carrier (1504) in relation to        the sheathing (1505) around the longitudinal centre line (1508)        of the pin (1502) and, on the other hand, to allow axial        shifting of the carrier (1504) in relation to the sheathing        (1505).        129. Applicator according to clause 128, wherein the carrier        (1504), on the distal end thereof, comprises a nose part (1506)        tapering in the distal direction with a rounded point (1509).        130. Applicator according to one of clauses 128-129, wherein the        carrier part has a carrier surface facing radially outwards, the        outer contour of which matches the inner contour of the        sheathing.        131. Applicator according to one of clauses 128-130, wherein the        tube (1501) and the pin (1502) are designed to be flexible, such        as bendable or kinkable, over at least a part of the length        thereof, in such a way that the longitudinal centre line of the        tube (1501) and pin (1502) is flexible, such as bendable or        kinkable.        132. Applicator according to one of clauses 128-131, wherein the        tube (1501) and the pin (1502), over at least a part of the        length thereof, are designed from superelastic material, such as        nitinol designed in superelastic form; and/or wherein the tube        (1501) and the pin (1502), over at least a part of the length        thereof, are designed as a wire, such as steel wire.        133. Assembly comprising, on the one hand, an applicator        according to one of clauses 128-132 and, on the other hand, an        aforementioned hollow prosthesis, in particular a heart        prosthesis, wherein the prosthesis is provided on the carrier in        a manner carried by the carrier.        134. Assembly according to clause 133 in combination with at        least clause 132, wherein the prosthesis is clamped on the        carrier surface (1510).        135. Assembly according to clause 133 or 134, wherein the        prosthesis is one from the group of:    -   a ring prosthesis according to one of clauses 75-100; and/or    -   a stent according to one of clauses 101-111; and/or    -   a ‘prosthesis of the type with a tubular element’.        136. Variable-diameter ring structure (1600) with distal (1604)        and proximal (1603) flange feet,        wherein the ring structure has an axial direction (1605) and a        radial direction (R) transverse to the axial direction;        wherein the distal and proximal flange feet (1604, 1603) have a        radial position, in which the free ends (1606, 1607) of the        flange feet point in the radial direction for anchoring with        surrounding tissue (1608);        wherein the distal flange feet (1604) have an extended position,        in which the distal flange feet extend in the axial direction;        and        wherein the distal flange feet (1604), if they are in the        extended position, are under a pre-tension (1609), which, when        released, bends the distal flange feet from the extended        position to the radial position; and        wherein the ring structure (1600) is constructed from a series        of elongated closed loops (1610) lying next to one another        which, in each case, at the midpoint of the longitudinal sides        thereof, are attached laterally to one another via a junction        (1611) to form this ring structure, in such a way that, on the        one hand, the imaginary line (1612) through all junctions (1611)        forms a closed ring and divides each loop (1610) into an        aforementioned distal flange foot (1601) and an aforementioned        proximal flange foot (1602) and, on the other hand, the ring        structure is expandable and/or compressible.        137. Ring structure (1600) according to clause 136, wherein the        distal flange feet (1604) are bendable from the radial position        to the extended position against a resilience which builds up        the aforementioned pre-tension (1609).        138. Ring structure (1600) according to one of clauses 136-137,        wherein the proximal flange feet (1603) have an extended        position, in which the proximal flange feet extend in the axial        direction (1605); and        wherein the proximal flange feet, if they are in the extended        position, are under a pre-tension (1609), which, when released,        bends the proximal flange feet (1603) from the extended position        to the radial position.        139. Ring structure (1600) according to clause 138, wherein the        proximal flange feet (1603) are bendable from the radial        position to the extended position against a resilience which        builds up the aforementioned pre-tension (1609).        140. Ring structure (1600) according to one of clauses 136-139,        wherein the ring structure is made from a memory material.        141. Ring structure (1600) according to clause 140, wherein the        memory material is a memory metal, such as a nitinol alloy.        142. Ring structure (1600) according to one of clauses 136-140,        wherein the ring structure is expandable from a first condition        (X1) to a second condition (X2), and wherein the ring structure,        when it is in the first condition, is under a radial pre-tension        (1613), which, when released, causes the ring structure to        expand in the direction of the second condition.        143. Ring structure (1600) according to one of clauses 136-141,        wherein the ring structure is expandable from a first condition        (X1) to a second condition (X2), and wherein the ring structure,        when it is in the second condition, is under a pre-tension,        which, when released, causes the ring structure to contract in        the direction of the first condition (X1).        144. Ring structure (1600) according to one of clauses 137-143,        wherein one or more of the junctions (1611) is provided with one        or more radial bores (1614).        145. Ring structure (1600) according to clause 144, wherein at        least 3, such as 4 or 8, junctions (1611) lying over the        circumference of the ring structure have one or more        aforementioned radial bores (1614).        146. Ring structure (1600) according to clause 144 of 145,        wherein all junctions have one or more aforementioned radial        bores (1614).        147. Ring structure (1600) according to one of clauses 134-146,        wherein the distal flange feet (1604), in the radial position,        show a bulge (1615) facing towards the proximal flange feet        (1603);        or        wherein the proximal flange feet, in the radial position, show a        bulge facing towards the distal flange feet;        148. Ring structure (1600) according to clause 147, wherein        these bulges (1615) are provided in the halves (1616) of the        respective flange feet adjacent to the junction (1611).        149. Ring structure (1600) according to one of clauses 136-148,        wherein the ring structure comprises a single piece of material.        150. Ring structure (1600) according to clause 149, wherein the        ring structure is made from a piece of tubular or otherwise        plate material.        151. Ring structure (1600) according to one of clauses 136-150,        wherein the ring structure is sterile.        152. Ring structure (1600) according to one of clauses 136-151,        wherein the ring structure is made from one or more medically        acceptable materials.        153. Ring structure (1600) according to one of clauses 136-152,        wherein one or more of the flange feet comprise one or more pins        on the sides facing towards one another.        154. Ring structure (1600) according to one of clauses 136-153,        wherein the ring structure or one or more flanges thereof, or        one or more flange feet thereof are totally or partially coated        in a sealing manner with tissue, such as pericardium, or        materials, such as textile or plastics which can be tolerated by        the body, such as Dacron and Teflon, which prevent the passage        of blood or other fluids.        155. Ring structure (1600) according to one of clauses 136-153,        wherein one or both flanges, or the flange feet of one or both        flanges thereof, differ from one another in length and/or in        width and/or in shape and/or in angle in relation to the        longitudinal axis, and/or manner of coating and/or filling.        156. Ring structure (1600) according to one of clauses 136-155,        wherein the separate flanges, or parts thereof, or the separate        flange feet of the separate flanges have an unequal shape and/or        length and/or width in relation to one another, and/or angle in        relation to the longitudinal axis, and/or fillings.        157. Ring structure (1600) according to clauses 136-156, wherein        the fillings of the separate flanges, or the separate flange        feet of the separate flanges, may have an unequal shape and/or        length and/or width in relation to one another, and/or angle in        relation to the longitudinal axis, and/or consistency and/or        material properties.        158. Ring structure (1600) according to clauses 136-157, wherein        the fillings of the separate flange feet extend beyond the        circumference of a flange foot, and/or in a lateral and/or        radial direction therefrom.        159. Ring structure (1600) according to clauses 136-158, wherein        the fillings of the separate flange feet are interconnected in        such a way that a continuity arises between all or a number of        fillings of the flange feet of one or both flanges.        160. Assembly comprising a ring structure (1600) according to        one of clauses 132-149, and a heart valve (1617) mounted        therein.        161. Assembly according to clause 150, wherein the heart valve        (1617) is a natural donor valve, such as from an animal or        human.        162. Assembly according to clause 150 or 151, wherein the heart        valve (1617) comprises a biological material, which is chosen        from the group of:    -   porcine valves; and/or    -   bovine valves; and/or    -   equine valves; and/or    -   human valves; and/or    -   kangaroo valves.        163. Manipulator (1700) for releasing a prosthesis (1701),        wherein the prosthesis has a plurality of distal (1702) and        proximal (1703) flange feet, which:    -   have a radial position, in which the free ends (1704, 1705) of        the flange feet point in the radial direction for anchoring with        surrounding tissue (1706);    -   have an extended position, in which the flange feet extend in        the radial direction; and,    -   if they are in the extended position, are under a pre-tension,        which, when released, bends the distal flange feet from the        extended position to the radial position;        wherein the manipulator (1700) comprises:    -   a plurality of U-shaped obstacle elements (1710) with a first        leg (1711) and a second leg (1712), the free ends (1713, 1714)        of which point in the distal direction (D);    -   an operating element (1715);    -   for each obstacle element (1714), a cord (1716), one end of        which is attached to the obstacle element (1710) and the other        end of which is connected to the operating element (1715) in        such a way that, when the operating element (1715) is displaced        in the proximal direction (P), the obstacle elements (1710) are        retracted in the proximal direction.        164. Manipulator (1700) according to clause 163,        wherein a first length (L1) is defined as the axial distance, in        the extended condition of the flange feet, between the free ends        (1704 and 1705) of the distal and proximal flange feet;        wherein the first legs (1711) of the obstacle elements have a        second length (L2); and        wherein the second length (L2) is at least 75%, such as at least        90%, of the first length (L1).        165. Manipulator (1700) according to clause 164, wherein the        second length (L2) is greater than the first length (L1).        166. Manipulator (1700) according to one of clauses 163-165,        wherein the second legs (1712) are shorter than the first legs        (1711).        167. Manipulator (1700) according to one of clauses 163-166,        wherein the proximal flange feet have a third length (L3),        wherein the second legs (1712) have a fourth length (L4); and        wherein the fourth length (L4) is at most equal to the third        length (L3).        168. Manipulator (1700) according to clause 167, wherein the        fourth length (L4) is at least 75% of the third length (L3).        169. Assembly comprising a manipulator (1700) according to one        of clauses 163-168 and a prosthesis (1701),        wherein the prosthesis has a plurality of distal (1702) and        proximal (1703) flange feet, which:    -   have a radial position, in which the free ends (1704, 1705) of        the flange feet point in the radial direction for anchoring with        surrounding tissue (1706);    -   have an extended position, in which the flange feet extend in        the axial direction; and,    -   if they are in the extended position, are under a pre-tension,        which, when released, bends the distal flange feet from the        extended position to the radial position.        170. Assembly according to clause 169, wherein a heart valve is        mounted in the prosthesis.        171. Assembly according to clause 170, wherein the heart valve        is a natural donor valve, such as from an animal or human.        172. Assembly according to clause 170 or 171, wherein the heart        valve comprises a biological material, which is chosen from the        group of:    -   porcine valves; and/or    -   bovine valves; and/or    -   equine valves; and/or    -   human valves; and/or    -   kangaroo valves.        173. Assembly according to one of clauses 169-172, wherein the        prosthesis is one from the group of:    -   a ring prosthesis (800) according to one of clauses 75-100;        and/or    -   a stent (90, 96) according to one of clauses 101-111; and/or    -   a ring structure according to one of clauses 136-162; and/or    -   a stented valve prosthesis; and/or    -   a ‘prosthesis of the type with a tubular element’.        174. Assembly according to one of clauses 166-170, wherein the        assembly further comprises a sleeve with a diameter smaller than        the maximum or expanded diameter of the prosthesis.        175. Port assembly (1800), comprising:    -   an annular connector (1802) which surrounds a port passage        (1830); and    -   a sealing cap (1803) to seal the port passage;        wherein the port passage extends from a first connector end        (1828) to a second connector end (1827);        wherein the second connector end comprises a crosswise contact        surface (1828) to lie against a wall (1829) of an organ;        wherein, in the crosswise contact surface, at least one adhesive        slot (1808, 1810), such as two adhesive slots, is provided,        which extends around the port passage (1830) and which is        connectable via a feed channel (1812) which opens out into this        slot to a source for tissue adhesive; and        wherein, in the crosswise contact surface (1828), at least one        ring, such as two rings, of one or more suction mouths (1809) is        provided, said ring extending around the port passage and being        connectable via a suction channel (1811) to a suction source to        suck the crosswise contact surface firmly against the wall of        the organ.        176. Port assembly (1800) according to clause 175, wherein the        connector (1802) and sealing cap (1803) are provided with a        first mating interlocking mechanism (1804, 1805), such as a        bayonet connection or screw thread, with which the connector and        sealing cap are attachable to one another in a manner which        seals the port passage.        177. Port assembly (1800) according to clause 176, wherein the        first mating interlocking mechanism comprises an inner screw        thread (1805) provided on the connector (1802) and an outer        screw thread (1804) provided on the closing cap (1803).        178. Port assembly (1800) according to one of clauses 175-177,        wherein the at least one ring of suction mouths comprises at        least one suction slot (1809), such as two suction slots, which        extend around the port passage (1830).        179. Port assembly (1800) according to one of the preceding        clauses 175-178, further comprising an adhesive source for        tissue adhesive and/or a suction source to generate a suction        force in the at least one ring of one or more suction mouths        (1808).        180. Port assembly (1800) according to one of the preceding        clauses 175-179, further comprising a work channel (1820, 1822)        which is connectable in a disconnectable manner to the connector        (1802).        181. Port assembly (1800) according to clause 180, wherein the        work channel comprises a stiff or stiffened channel part (1822)        and a flexible channel part (1820) which is provided between the        connector (1802) and the stiff channel part (1822) in such a way        that the stiff channel part is pivotable in relation to the        connector.        182. Port assembly (1850), comprising:    -   an annular connector (1802) which surrounds a port passage        (1830), said port passage extending from a first connector end        (1828) to a second connector end (1827); and    -   a work channel (1820, 1822) which is connectable in a        disconnectable manner to the connector (1802);        wherein the second connector end (1827) comprises a crosswise        contact surface (1828) to lie against a wall (1829) of an organ;        and        wherein the work channel comprises a stiff or stiffened channel        part (1822) and a flexible channel part (1820) which is provided        between the connector (1802) and the stiff channel part (1822)        in such a way that the stiff channel part (1822) is pivotable in        relation to the connector (1802).        183. Port assembly (1850) according to clause 182, wherein the        assembly further comprises a closing cap (1803) to close the        port passage (1830).        184. Port assembly (1800, 1850) according to one of clauses        180-183, wherein the connector (1802) and the work channel        (1820, 1822) are provided with a second mating interlocking        mechanism (1806, 1807), such as a bayonet connection or screw        thread, with which the connector and the work channel are        attachable to one another in a sealing manner.        185. Port assembly (1800, 1850) according to clause 184, wherein        the second mating interlocking mechanism comprises an outer        screw thread (1806) provided on the connector and an inner screw        thread (1807) provided on the closing cap.        186. Port assembly (1800, 1850) according to one of clauses        180-185, wherein the end of the work channel facing away from        the connector is provided with a seal (1824) which is designed,        on the one hand, to seal the access to the passage surrounded by        the work channel and, on the other hand, to allow through an        instrument which is to be inserted inwards into the work        channel, while maintaining the seal.        187. Port assembly (1800, 1850) according to one of the        preceding clauses 180-186, wherein the work channel is provided        with at least one connection, such as two, three or four        connections, for gassing and/or degassing and/or irrigation        and/or drainage of the passage surrounded by the work channel.        188. Port assembly (1800, 1850) according to one of the        preceding clauses 180-187, wherein one or more valves are        provided in the work channel.        189. Port assembly (1800, 1850) according to one of the        preceding clauses 175-188, wherein the connector is made from        soluble, so-called ‘bioabsorbable’ or ‘biodegradable’ materials.        190. Port assembly (1800, 1850) according to one of clauses        175-189,        wherein the cap is coated on the crosswise side with        anti-thrombotic materials or chemical components to prevent        blood clotting in situ; or        wherein the cap is covered on the crosswise side with a piece of        a vascular prosthesis, human pericardium, or other material to        promote the growth of endothelial tissue in situ.        191. Port assembly (1800, 1850) according to one of clauses        175-190, wherein the connector is provided with one or more        contact and/or pressure sensors on the crosswise edge.        192. Method for implanting a valve prosthesis in a passage        through which blood flows, comprising the following steps:    -   the insertion into the passage and attachment to surrounding        tissue of a ring prosthesis which, under pre-tension, is held in        a first diameter, wherein the pre-tension tends to constrict the        ring prosthesis to a smaller, second diameter;    -   the insertion into the passage of the valve prosthesis;    -   the release of the pre-tensioned ring prosthesis in such a way        that, under the influence of the pre-tension, it draws the        tissue surrounding the passage against the valve prosthesis.        193. Method according to clause 192, wherein the step of        implantation and attachment of the ring prosthesis in the        passage takes place prior to the step of implantation of the        valve prosthesis in the passage.        194. Method according to clause 192, wherein the step of        implantation of the valve prosthesis in the passage takes place        prior to the step of implantation and attachment of the ring        prosthesis in the passage.        195. Method according to clause 192, wherein the steps of, on        the one hand, implantation and attachment of the ring prosthesis        in the passage and, on the other hand, of implantation of the        valve prosthesis in the passage take place simultaneously.        196. Method according to clause 195, wherein the ring prosthesis        and valve prosthesis are implanted and attached as a        pre-assembled unit.        197. Method according to one of clauses 192-196, wherein the        valve prosthesis is implanted within the lumen surrounded by the        ring prosthesis or is provided within the lumen surrounded by        the ring prosthesis.        198. Method according to one of clauses 192-197, wherein the        ring prosthesis is one from the group comprising:    -   ring prostheses according to one of clauses 75-100; or    -   ring structures according to one of clauses 136-159.        199. Valve prosthesis, such as a heart valve prosthesis,        comprising:    -   at least a first radial flange provided with radial slots;    -   pins which project in an axial direction through the slots;    -   a tensioning mechanism designed to be able to pre-tension the        pins in order to move through the slots in a radially inward        direction; and    -   a valve, such as a heart valve.        200. Valve prosthesis according to clause 199, further        comprising a ring prosthesis according to one of clauses 75-100,        wherein the pins are mounted on the waved wire of this ring        prosthesis, and wherein the waved wire can be pre-tensioned in        order to drive the pins in a radially inward direction through        the slots.        201. Valve prosthesis according to one of clauses 199-201,        wherein the tensioning mechanism comprises, for each slot, a        radially oriented spring which grips on an aforementioned pin.        202. Valve prosthesis according to one of clauses 199-201,        wherein the first flange is constructed from a plurality of        flange feet with an aforementioned slot.        203. Valve prosthesis according to one of clauses 199-202,        wherein the tensioning mechanism is housed in a cavity formed in        the first flange, or cavities formed in flange feet and, and        wherein the slots open out into this cavity/these cavities.        204. Valve prosthesis according to clause 203, wherein the        cavity is formed by designing the first flange as double-walled        (or the cavities are formed by designing the flange feet as        double-walled).        205. Valve prosthesis according to one of clauses 199-204,        wherein the first flange is movable from an extended position,        in which the first flange is axially oriented and the pins are        radially oriented, to a radial position, in which the first        flange is radially oriented and the pins are axially oriented.        206. Valve prosthesis according to one of the preceding clauses        199-205, further comprising a second radial flange in order to        be able to grip, together with the first radial flange, on        tissue, such as annulus tissue, located between the first and        second flange, and wherein, if the first flange and second        flange are radially oriented, the pins extend from the first        flange in the direction of the second flange.        207. Valve prosthesis according to clause 206, wherein the        second flange is movable from an extended position, in which the        second flange is axially oriented, to a radial position, in        which the second flange is radially oriented.

What is claimed is:
 1. An atrioventricular valve prosthesis forattachment in a valve passage surrounded by tissue, the atrioventricularvalve prosthesis comprising: a tubular valve support frame with an opengrid structure, said support frame having a proximal end facing in aproximal direction, a distal end facing in a distal direction, an axialcenter line extending in an axial direction of the support frame, and anoutside surface, the proximal end and distal end being spaced apart fromone another along the axial direction, and the outside surface beingdefined as a surface of the support frame facing away from the axialcenter line; a heart valve provided inside said support frame; anannular series of proximal anchors surrounding said support frame, eachof said proximal anchors having one secured outer end secured to saidsupport frame and one free outer end; and an annular series of distalanchors surrounding said support frame, each of said distal anchorshaving one secured outer end secured to said support frame and one freeouter end; wherein said support frame is expansible from a compressedconfiguration to an expanded configuration; wherein in said expandedconfiguration said support frame has an enlarged extent relative to saidcompressed configuration in a radial direction that is perpendicular tosaid axial direction; wherein said proximal anchors and said distalanchors are configured to move from a first condition associated to saidcompressed configuration of said support frame to a second conditionassociated to said expanded configuration of said support frame, suchthat said proximal anchors and said distal anchors extend radiallyoutwardly of said support frame in said second condition to a greaterextent than in said first condition, said proximal anchors and saiddistal anchors being in the first condition when navigating theprosthesis to an intended location in a body of a patient; wherein saidsecured outer ends of said annular series of proximal anchors and saidsecured outer ends of said annular series of distal anchors are, viewedalong said axial direction, provided at positions intermediate saidproximal end and said distal end of said support frame, such that saidsecured outer ends of the proximal anchors and of the distal anchors arearranged spaced apart from the proximal end of said support frame aswell as from the distal end of said support frame; and wherein saidproximal anchors and said distal anchors lie, when said proximal anchorsand said distal anchors are in said first condition, in the axialdirection along the outside surface of said support frame with the freeouter ends of the proximal anchors pointing in the proximal directionand with the free outer ends of the distal anchors pointing in thedistal direction such that, when the proximal anchors and distal anchorsmove from the first condition to the second condition, the proximal anddistal anchors move towards each other to clamp surrounding tissuelocated between the proximal and distal anchors.
 2. The prosthesisaccording to claim 1, wherein said heart valve is a mitral valve.
 3. Theprosthesis according to claim 1, wherein said heart valve is compressedwhen said support frame is in said compressed configuration and isexpansible when said support frame expands.
 4. The prosthesis accordingto claim 1, wherein, said tubular valve support frame has a first zonewith a first diameter and a second zone with a second diameter, thefirst diameter being smaller than the second diameter; and said annularseries of proximal anchors and said annular series of distal anchors areprovided in one of: the first zone or second zone.
 5. The prosthesisaccording to claim 1, wherein said proximal anchors and said distalanchors are under a pretension when in said first condition, thepretension acting to move said proximal anchors and said distal anchorsto said second condition upon release of said pretension.
 6. Theprosthesis according to claim 5, wherein said tubular valve supportframe, said proximal anchors and said distal anchors are made from amemory material.
 7. The prosthesis according to claim 1, wherein, saiddistal anchors, at said secured outer ends, are provided with a fillingon a side facing opposite proximal anchors, and/or said proximalanchors, at said secured outer ends, are provided with a filling on aside facing opposite distal anchors; wherein said filling of said distaland/or proximal anchors, respectively, is designed, in said secondcondition of said distal and proximal anchors, to increase a clampingforce with which said distal and proximal anchors clamp the tissue insitu; wherein said distal and/or proximal anchors, respectively, have aconcave-curved part which follows on from said secured outer ends of thedistal and/or proximal anchors, respectively, secured to said supportframe, a hollow side of said concave-curved part facing towards saidproximal and/or distal anchors, respectively; and wherein said fillingof said distal and/or proximal anchors, respectively, is provided insaid hollow side of said concave-curved part.
 8. The prosthesisaccording to claim 7, wherein said concave-curved part of said distaland/or proximal anchors, respectively, on a side of said concave-curvedpart, which faces towards said free outer ends of said distal and/orproximal anchors, respectively, viewed in said radial direction and saidsecond condition, changes to a straight part.
 9. The prosthesisaccording to claim 1, further comprising a ring structure providing saidannular series of proximal anchors and said annular series of distalanchors; wherein said ring structure is constructed from a series ofelongated closed loops lying next to one another, which loops, at themidpoint of longitudinal sides thereof, are attached laterally to oneanother via a junction to form said ring structure, in such a way thata) an imaginary center line through all junctions forms a closed ringand divides each loop into a distal anchor of the annular series ofdistal anchors and a proximal anchor of the annular series of proximalanchors, and that b) said ring structure is expandable and/orcompressible; said proximal anchors and said distal anchors, when insaid first condition, are under a pre-tension, which upon release ofsaid pre-tension, bends said proximal anchors and said distal anchorsfrom said first condition to said second condition.
 10. The prosthesisaccording to claim 9, wherein said distal anchors, in said secondcondition, show a bulge facing towards said proximal anchors; or whereinsaid proximal anchors, in said second condition, show a bulge facingtowards said distal anchors.
 11. A method of implanting anatrioventricular valve prosthesis in a passage between an atrium and aventricle, the method comprising steps of: navigating a prosthesisaccording to claim 1, having said support frame in said compressedconfiguration and said proximal anchors and said distal anchors in saidfirst condition, to the passage; inserting said prosthesis into thepassage; expanding said support frame to said expanded configuration;and attaching said prosthesis to tissue surrounding the passage bybending said proximal anchors and said distal anchors towards each otherfrom said first condition to said second condition and clamping thetissue surrounding the passage between said proximal anchors and saiddistal anchors.
 12. Assembly comprising a prosthesis according to claim1 and a mechanical obstacle holding the proximal and distal anchors inthe first condition, wherein the mechanical obstacle is movable withrespect to the support frame to release the proximal and distal anchorsfor moving the proximal and distal anchors from the first condition tothe second condition.
 13. Assembly according to claim 12, wherein themechanical obstacle is a tube.
 14. An atrioventricular valve prosthesis,comprising: a tubular valve support frame with an open grid structure,said support frame having a proximal end facing in a proximal direction,a distal end facing in a distal direction, an axial center lineextending in an axial direction of the support frame, and an outsidesurface, the proximal end and distal end being spaced apart from oneanother along the axial direction, and the outside surface being definedas a surface of the support frame facing away from the axial centerline; a heart valve provided inside said support frame; a proximalanchor annularly surrounding said support frame, said proximal anchorhaving one secured outer end secured to said support frame and one freeouter end; and a distal anchor annularly surrounding said support frame,said distal anchor having one secured outer end secured to said supportframe and one free outer end; wherein said support frame is expansiblefrom a compressed configuration to an expanded configuration, wherein insaid expanded configuration said support frame has an enlarged extentrelative to said compressed configuration in a radial direction that isperpendicular to said axial direction; wherein said proximal anchor andsaid distal anchor are configured to move from a first conditionassociated to said compressed configuration to a second conditionassociated to said expanded configuration, such that said proximalanchor and said distal anchor extend radially outwardly of said supportframe in said second condition to a greater extent than in said firstcondition, said proximal anchor and said distal anchor being in thefirst condition when navigating the prosthesis to an intended locationin a body of a patient; wherein said secured outer end of said annularproximal anchor and said secured outer end of said annular distal anchorare, viewed along said axial direction, provided at positionsintermediate said proximal end and said distal end of said supportframe, such that said secured outer end of the proximal anchor and ofthe distal anchor are arranged spaced apart from the proximal end ofsaid support frame as well as from the distal end of said support frame;and wherein said proximal anchor and said distal anchor lie, when saidproximal anchor and said distal anchor are in said first condition, inthe axial direction along the outside surface of said support frame withthe free outer end of the proximal anchor pointing in the proximaldirection and with the free outer end of the distal anchor pointing inthe distal direction such that, when the proximal anchor and distalanchor move from the first condition to the second condition, theproximal and distal anchors move towards each other to clamp surroundingtissue between the proximal and distal anchors.
 15. The prosthesisaccording to claim 14, wherein said heart valve is a mitral valve. 16.The prosthesis according to claim 14, wherein said heart valve iscompressed when said support frame is in said compressed configurationand is expansible when said support frame expands.
 17. The prosthesisaccording to claim 14, wherein said tubular valve support frame has afirst zone with a first diameter and a second zone with a seconddiameter, the first diameter being smaller than the second diameter; andwherein said proximal anchor and said distal anchor are provided in oneof: the first zone or second zone.
 18. The prosthesis according to claim14, wherein said proximal anchor and said distal anchor are under apretension when in said first condition, the pretension acting to movesaid proximal anchor and said distal anchor to said second conditionupon release of said pretension.
 19. The prosthesis according to claim18, wherein said tubular support valve frame, said proximal anchor andsaid distal anchor are made from a memory material.
 20. The prosthesisaccording to claim 14, wherein, said distal anchor, at said securedouter end, is provided with a filling on a side facing the proximalanchor, and/or said proximal anchor, at said secured outer end, isprovided with a filling on a side facing the distal anchor; wherein saidfilling of said distal and/or proximal anchor, respectively, isdesigned, in said second condition of said distal and proximal anchor,to increase a clamping force with which said distal and proximal anchorclamp the tissue in situ; wherein said distal and/or proximal anchor,respectively, have a concave-curved part which follows on from saidsecured outer end of the distal and/or proximal anchor, respectively, ahollow side of said concave-curved part facing towards said proximaland/or distal anchor, respectively; and wherein said filling of saiddistal and/or proximal anchor, respectively, is provided in said hollowside of said concave-curved part.
 21. The prosthesis according to claim20, wherein said concave-curved part of said distal and/or proximalanchor, respectively, on a side thereof facing towards said free outerend of said distal and/or proximal anchor, respectively, viewed in saidradial direction and said second condition, changes to a straight part.22. Assembly comprising a prosthesis according to claim 14 and amechanical obstacle holding the proximal and distal anchors in the firstcondition, wherein the mechanical obstacle is movable with respect tothe support frame to release the proximal and distal anchors for movingthe proximal and distal anchors from the first condition to the secondcondition.
 23. Assembly according to claim 22, wherein the mechanicalobstacle is a tube.
 24. A method of implanting an atrioventricular valveprosthesis in a passage between an atrium and a ventricle, the methodcomprising steps of: navigating a prosthesis according to claim 14,having said support frame in said compressed configuration and saidproximal anchor and said distal anchor in said first condition, to thepassage; inserting said prosthesis into the passage; expanding saidsupport frame to said expanded configuration; and attaching saidprosthesis to tissue surrounding the passage by bending said proximalanchor and said distal anchor towards each other from said firstcondition to said second condition and clamping the tissue surroundingthe passage between said proximal anchor and said distal anchor.